Canonical Allele Identifier: CA3310097

Gene: POLK

Linked Data

• dbSNP Id: rs764419171
• ExAC: 5:74893597 T / C
• gnomAD v2: 5-74893597-T-C
• gnomAD v4: 5-75597772-T-C
• MyVariant Identifiers: chr5:g.74893597T>C (hg19) ; chr5:g.75597772T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597772T>C , CM000667.2:g.75597772T>C	GRCh38
NC_000005.9:g.74893597T>C , CM000667.1:g.74893597T>C	GRCh37
NC_000005.8:g.74929353T>C	NCBI36
NG_051590.1:g.91023T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241436.9:c.2511T>C MANE Select	ENSP00000241436.4:p.Ala837=
ENST00000241436.8:c.2511T>C	ENSP00000241436.4:p.Ala837=
ENST00000502567.1:n.356T>C
ENST00000503479.6:c.*1034T>C	ENSP00000421997.2:n.*1034T>C
ENST00000504026.5:c.1382T>C	ENSP00000425075.1:p.Leu461Pro
ENST00000505069.1:n.91T>C
ENST00000505975.5:c.2625T>C	ENSP00000424859.1:n.2625T>C
ENST00000506928.5:n.2634T>C
ENST00000508526.5:c.1917T>C	ENSP00000426853.1:p.Ala639=
ENST00000509126.2:c.2339T>C	ENSP00000423532.1:n.2339T>C
ENST00000510815.6:c.*1034T>C	ENSP00000422094.2:n.*1034T>C
ENST00000511527.5:c.1496T>C	ENSP00000420997.1:n.1496T>C
ENST00000514141.5:c.*1130T>C	ENSP00000423526.1:n.*1130T>C
NM_016218.2:c.2511T>C	NP_057302.1:p.Ala837=
XM_005248534.3:c.2553T>C	XP_005248591.1:p.Ala851=
XM_006714652.2:c.1266T>C	XP_006714715.1:p.Ala422=
XM_011543463.1:c.2553T>C	XP_011541765.1:p.Ala851=
XM_011543464.1:c.2553T>C	XP_011541766.1:p.Ala851=
XM_011543465.1:c.2553T>C	XP_011541767.1:p.Ala851=
XM_011543466.1:c.2553T>C	XP_011541768.1:p.Ala851=
XM_011543467.1:c.2283T>C	XP_011541769.1:p.Ala761=
XR_241784.1:n.2519T>C
XR_948273.1:n.2703T>C
NM_001345921.1:c.2313T>C	NP_001332850.1:p.Ala771=
NM_001345922.1:c.2241T>C	NP_001332851.1:p.Ala747=
NM_016218.3:c.2511T>C	NP_057302.1:p.Ala837=
NR_144315.1:n.2517T>C
XM_005248534.5:c.2553T>C	XP_005248591.1:p.Ala851=
XM_006714652.4:c.1266T>C	XP_006714715.1:p.Ala422=
XM_011543463.3:c.2553T>C	XP_011541765.1:p.Ala851=
XM_011543464.3:c.2553T>C	XP_011541766.1:p.Ala851=
XM_011543467.3:c.2283T>C	XP_011541769.1:p.Ala761=
XM_017009559.2:c.2511T>C	XP_016865048.1:p.Ala837=
XM_017009560.2:c.2511T>C	XP_016865049.1:p.Ala837=
XM_017009561.2:c.2355T>C	XP_016865050.1:p.Ala785=
XM_017009563.2:c.2241T>C	XP_016865052.1:p.Ala747=
XR_001742105.2:n.3001T>C
XR_001742107.2:n.3085T>C
XR_001742108.2:n.2619T>C
XR_241784.3:n.3043T>C
XR_948273.3:n.2703T>C
NM_001345921.2:c.2313T>C	NP_001332850.1:p.Ala771=
NM_001345922.2:c.2241T>C	NP_001332851.1:p.Ala747=
NM_001387110.2:c.2502T>C	NP_001374039.1:p.Ala834=
NM_001387111.2:c.2553T>C	NP_001374040.1:p.Ala851=
NM_001387113.2:c.2511T>C	NP_001374042.1:p.Ala837=
NM_016218.5:c.2511T>C	NP_057302.1:p.Ala837=
NR_144315.2:n.2376T>C
NR_170559.2:n.2365T>C
NR_170560.2:n.2597T>C
NM_001345921.3:c.2313T>C	NP_001332850.1:p.Ala771=
NM_001345922.3:c.2241T>C	NP_001332851.1:p.Ala747=
NM_001387110.3:c.2502T>C	NP_001374039.1:p.Ala834=
NM_001387111.3:c.2553T>C	NP_001374040.1:p.Ala851=
NM_001387113.3:c.2511T>C	NP_001374042.1:p.Ala837=
NM_001395893.1:c.2241T>C	NP_001382822.1:p.Ala747=
NM_001395894.1:c.2553T>C	NP_001382823.1:p.Ala851=
NM_001395897.1:c.2550T>C	NP_001382826.1:p.Ala850=
NM_001395899.1:c.2358T>C	NP_001382828.1:p.Ala786=
NM_001395900.1:c.2313T>C	NP_001382829.1:p.Ala771=
NM_001395901.1:c.2271T>C	NP_001382830.1:p.Ala757=
NM_001395902.1:c.2241T>C	NP_001382831.1:p.Ala747=
NM_016218.6:c.2511T>C MANE Select	NP_057302.1:p.Ala837=
NR_144315.3:n.2376T>C
NR_170559.3:n.2365T>C
NR_170560.3:n.2597T>C