Canonical Allele Identifier: CA366734808

Gene: PMS2

Linked Data

• MyVariant Identifiers: chr7:g.6013067C>A (hg19) ; chr7:g.5973436C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5973436C>A , CM000669.2:g.5973436C>A	GRCh38
NC_000007.13:g.6013067C>A , CM000669.1:g.6013067C>A	GRCh37
NC_000007.12:g.5979593C>A	NCBI36
NG_008466.1:g.40671G>T , LRG_161:g.40671G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699814.2:c.*1948G>T	ENSP00000514615.2:n.*1948G>T
ENST00000699840.2:c.2549G>T	ENSP00000514638.2:p.Arg850Ile
ENST00000699930.2:c.2444G>T	ENSP00000514695.2:p.Arg815Ile
ENST00000406569.8:c.1912G>T	ENSP00000514464.1:n.1912G>T
ENST00000644110.2:c.*2146G>T	ENSP00000496392.2:n.*2146G>T
ENST00000699752.1:c.2396G>T	ENSP00000514561.1:p.Arg799Ile
ENST00000699753.1:c.*1973G>T	ENSP00000514562.1:n.*1973G>T
ENST00000699754.1:c.2354G>T	ENSP00000514563.1:p.Arg785Ile
ENST00000699755.1:c.*1951G>T	ENSP00000514564.1:n.*1951G>T
ENST00000699756.1:c.*2139G>T	ENSP00000514565.1:n.*2139G>T
ENST00000699757.1:c.*1809G>T	ENSP00000514566.1:n.*1809G>T
ENST00000699758.1:c.*1809G>T	ENSP00000514567.1:n.*1809G>T
ENST00000699759.1:n.3406G>T
ENST00000699760.1:c.2234G>T	ENSP00000514568.1:p.Arg745Ile
ENST00000699761.1:c.2147G>T	ENSP00000514569.1:p.Arg716Ile
ENST00000699762.1:c.1979G>T	ENSP00000514570.1:p.Arg660Ile
ENST00000699763.1:c.*1642G>T	ENSP00000514571.1:n.*1642G>T
ENST00000699764.1:c.*870G>T	ENSP00000514572.1:n.*870G>T
ENST00000699765.1:c.*1547G>T	ENSP00000514573.1:n.*1547G>T
ENST00000699766.1:c.2585G>T	ENSP00000514574.1:p.Arg862Ile
ENST00000699767.1:c.*193G>T	ENSP00000514575.1:n.*193G>T
ENST00000699768.1:c.2408G>T	ENSP00000514576.1:p.Arg803Ile
ENST00000699811.1:c.2147G>T	ENSP00000514614.1:p.Arg716Ile
ENST00000699813.1:n.2665G>T
ENST00000699814.1:c.2175G>T
ENST00000699815.1:c.*2083G>T	ENSP00000514616.1:n.*2083G>T
ENST00000699816.1:c.*1442G>T	ENSP00000514617.1:n.*1442G>T
ENST00000699817.1:c.*2146G>T	ENSP00000514618.1:n.*2146G>T
ENST00000699818.1:c.2147G>T	ENSP00000514619.1:p.Arg716Ile
ENST00000699819.1:c.*1709G>T	ENSP00000514620.1:n.*1709G>T
ENST00000699820.1:c.*490G>T	ENSP00000514621.1:n.*490G>T
ENST00000699821.1:c.2180G>T	ENSP00000514622.1:p.Arg727Ile
ENST00000699822.1:c.*2004G>T	ENSP00000514623.1:n.*2004G>T
ENST00000699823.1:c.2147G>T	ENSP00000514624.1:p.Arg716Ile
ENST00000699824.1:c.*2055G>T	ENSP00000514625.1:n.*2055G>T
ENST00000699825.1:c.1991G>T	ENSP00000514626.1:p.Arg664Ile
ENST00000699826.1:c.*1951G>T	ENSP00000514627.1:n.*1951G>T
ENST00000699827.1:c.2384G>T	ENSP00000514628.1:p.Arg795Ile
ENST00000699828.1:c.*1642G>T	ENSP00000514629.1:n.*1642G>T
ENST00000699833.1:n.4324G>T
ENST00000699837.1:c.2147G>T	ENSP00000514635.1:p.Arg716Ile
ENST00000699838.1:c.*2452G>T	ENSP00000514636.1:n.*2452G>T
ENST00000699839.1:c.2738G>T	ENSP00000514637.1:p.Arg913Ile
ENST00000699916.1:c.*1809G>T	ENSP00000514684.1:n.*1809G>T
ENST00000699917.1:c.*2001G>T	ENSP00000514685.1:n.*2001G>T
ENST00000699918.1:c.*2053G>T	ENSP00000514686.1:n.*2053G>T
ENST00000699919.1:c.*2139G>T	ENSP00000514687.1:n.*2139G>T
ENST00000699920.1:c.*2188G>T	ENSP00000514688.1:n.*2188G>T
ENST00000699928.1:c.*490G>T	ENSP00000514693.1:n.*490G>T
ENST00000699951.1:c.*1605G>T	ENSP00000514706.1:n.*1605G>T
ENST00000699952.1:c.*106G>T	ENSP00000514707.1:n.*106G>T
ENST00000265849.12:c.2552G>T MANE Select	ENSP00000265849.7:p.Arg851Ile
ENST00000642292.1:c.2147G>T	ENSP00000495524.1:p.Arg716Ile
ENST00000642456.1:c.2147G>T	ENSP00000493814.1:p.Arg716Ile
ENST00000643595.1:c.*1951G>T	ENSP00000494497.1:n.*1951G>T
ENST00000644110.1:c.2234G>T	ENSP00000496392.1:p.Arg745Ile
ENST00000265849.11:c.2552G>T	ENSP00000265849.7:p.Arg851Ile
ENST00000382321.5:c.1349G>T	ENSP00000371758.4:p.Arg450Ile
ENST00000441476.6:c.2234G>T	ENSP00000392843.2:p.Arg745Ile
NM_000535.5:c.2552G>T , LRG_161t1:c.2552G>T	NP_000526.1:p.Arg851Ile
NR_003085.2:n.2634G>T
XM_006715742.2:c.2546G>T	XP_006715805.1:p.Arg849Ile
XM_006715744.2:c.1619G>T	XP_006715807.1:p.Arg540Ile
XM_011515427.1:c.2597G>T	XP_011513729.1:p.Arg866Ile
XM_011515428.1:c.2441G>T	XP_011513730.1:p.Arg814Ile
XM_011515429.1:c.2234G>T	XP_011513731.1:p.Arg745Ile
XM_011515430.1:c.2234G>T	XP_011513732.1:p.Arg745Ile
NM_000535.6:c.2552G>T	NP_000526.2:p.Arg851Ile
NM_001322003.1:c.2147G>T	NP_001308932.1:p.Arg716Ile
NM_001322004.1:c.2147G>T	NP_001308933.1:p.Arg716Ile
NM_001322005.1:c.2147G>T	NP_001308934.1:p.Arg716Ile
NM_001322006.1:c.2396G>T	NP_001308935.1:p.Arg799Ile
NM_001322007.1:c.2234G>T	NP_001308936.1:p.Arg745Ile
NM_001322008.1:c.2234G>T	NP_001308937.1:p.Arg745Ile
NM_001322009.1:c.2180G>T	NP_001308938.1:p.Arg727Ile
NM_001322010.1:c.1991G>T	NP_001308939.1:p.Arg664Ile
NM_001322011.1:c.1619G>T	NP_001308940.1:p.Arg540Ile
NM_001322012.1:c.1619G>T	NP_001308941.1:p.Arg540Ile
NM_001322013.1:c.1979G>T	NP_001308942.1:p.Arg660Ile
NM_001322014.1:c.2585G>T	NP_001308943.1:p.Arg862Ile
NM_001322015.1:c.2243G>T	NP_001308944.1:p.Arg748Ile
NR_136154.1:n.2596G>T
XM_006715744.4:c.1619G>T	XP_006715807.1:p.Arg540Ile
XM_017012342.2:c.1619G>T	XP_016867831.1:p.Arg540Ile
XM_024446800.1:c.1991G>T	XP_024302568.1:p.Arg664Ile
NM_000535.7:c.2552G>T MANE Select	NP_000526.2:p.Arg851Ile
NM_001322003.2:c.2147G>T	NP_001308932.1:p.Arg716Ile
NM_001322004.2:c.2147G>T	NP_001308933.1:p.Arg716Ile
NM_001322005.2:c.2147G>T	NP_001308934.1:p.Arg716Ile
NM_001322006.2:c.2396G>T	NP_001308935.1:p.Arg799Ile
NM_001322008.2:c.2234G>T	NP_001308937.1:p.Arg745Ile
NM_001322009.2:c.2180G>T	NP_001308938.1:p.Arg727Ile
NM_001322010.2:c.1991G>T	NP_001308939.1:p.Arg664Ile
NM_001322011.2:c.1619G>T	NP_001308940.1:p.Arg540Ile
NM_001322012.2:c.1619G>T	NP_001308941.1:p.Arg540Ile
NM_001322013.2:c.1979G>T	NP_001308942.1:p.Arg660Ile
NM_001322014.2:c.2585G>T	NP_001308943.1:p.Arg862Ile
NM_001322015.2:c.2243G>T	NP_001308944.1:p.Arg748Ile
NM_001322007.2:c.2234G>T	NP_001308936.1:p.Arg745Ile