Canonical Allele Identifier: CA345375033

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237016264G>T (hg19) ; chr1:g.236852964G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852964G>T , CM000663.2:g.236852964G>T	GRCh38
NC_000001.10:g.237016264G>T , CM000663.1:g.237016264G>T	GRCh37
NC_000001.9:g.235082887G>T	NCBI36
NG_008959.1:g.62684G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1829G>T MANE Select	ENSP00000355536.5:p.Gly610Val
ENST00000535889.6:c.1829G>T	ENSP00000441845.1:p.Gly610Val
ENST00000650888.1:c.*871G>T	ENSP00000498393.1:n.*871G>T
ENST00000651455.1:c.*573G>T	ENSP00000498963.1:n.*573G>T
ENST00000674797.2:c.1481G>T	ENSP00000502299.2:p.Gly494Val
ENST00000679569.1:n.2143G>T
ENST00000679842.1:c.1829G>T	ENSP00000506109.1:p.Gly610Val
ENST00000680454.1:n.2273G>T
ENST00000681102.1:c.1649G>T	ENSP00000505600.1:p.Gly550Val
ENST00000681177.1:c.1516-6869G>T	ENSP00000506327.1:n.1516-6869G>T
ENST00000681937.1:n.2148-6869G>T
ENST00000366576.3:c.491G>T	ENSP00000355535.3:p.Gly164Val
ENST00000366577.9:c.1829G>T	ENSP00000355536.5:p.Gly610Val
ENST00000463959.1:n.1848G>T
ENST00000535889.5:c.1829G>T	ENSP00000441845.1:p.Gly610Val
NM_000254.2:c.1829G>T	NP_000245.2:p.Gly610Val
NM_001291939.1:c.1829G>T	NP_001278868.1:p.Gly610Val
NM_001291940.1:c.608G>T	NP_001278869.1:p.Gly203Val
XM_005273141.3:c.1826G>T	XP_005273198.1:p.Gly609Val
XM_006711769.2:c.1829G>T	XP_006711832.1:p.Gly610Val
XM_006711770.1:c.893G>T	XP_006711833.1:p.Gly298Val
XM_011544193.1:c.1829G>T	XP_011542495.1:p.Gly610Val
XM_011544194.1:c.1997G>T	XP_011542496.1:p.Gly666Val
XM_005273141.5:c.1826G>T	XP_005273198.1:p.Gly609Val
XM_006711770.3:c.893G>T	XP_006711833.1:p.Gly298Val
XM_011544194.3:c.1997G>T	XP_011542496.1:p.Gly666Val
XM_017001329.2:c.1997G>T	XP_016856818.1:p.Gly666Val
XM_017001330.2:c.1997G>T	XP_016856819.1:p.Gly666Val
NM_001291940.2:c.608G>T	NP_001278869.1:p.Gly203Val
NM_000254.3:c.1829G>T MANE Select	NP_000245.2:p.Gly610Val