Canonical Allele Identifier: CA423811498

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237015901A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852601A>G , CM000663.2:g.236852601A>G	GRCh38
NC_000001.10:g.237015901A>G , CM000663.1:g.237015901A>G	GRCh37
NC_000001.9:g.235082524A>G	NCBI36
NG_008959.1:g.62321A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1776A>G MANE Select	ENSP00000355536.5:p.Glu592=
ENST00000535889.6:c.1776A>G	ENSP00000441845.1:p.Glu592=
ENST00000650888.1:c.*818A>G	ENSP00000498393.1:n.*818A>G
ENST00000651455.1:c.*520A>G	ENSP00000498963.1:n.*520A>G
ENST00000674797.2:c.1428A>G	ENSP00000502299.2:p.Glu476=
ENST00000679569.1:n.2090A>G
ENST00000679842.1:c.1776A>G	ENSP00000506109.1:p.Glu592=
ENST00000680454.1:n.2220A>G
ENST00000681102.1:c.1596A>G	ENSP00000505600.1:p.Glu532=
ENST00000681177.1:c.1516-7232A>G	ENSP00000506327.1:n.1516-7232A>G
ENST00000681937.1:n.2148-7232A>G
ENST00000366576.3:c.438A>G	ENSP00000355535.3:p.Glu146=
ENST00000366577.9:c.1776A>G	ENSP00000355536.5:p.Glu592=
ENST00000463959.1:n.1795A>G
ENST00000535889.5:c.1776A>G	ENSP00000441845.1:p.Glu592=
NM_000254.2:c.1776A>G	NP_000245.2:p.Glu592=
NM_001291939.1:c.1776A>G	NP_001278868.1:p.Glu592=
NM_001291940.1:c.555A>G	NP_001278869.1:p.Glu185=
XM_005273141.3:c.1773A>G	XP_005273198.1:p.Glu591=
XM_006711769.2:c.1776A>G	XP_006711832.1:p.Glu592=
XM_006711770.1:c.840A>G	XP_006711833.1:p.Glu280=
XM_011544193.1:c.1776A>G	XP_011542495.1:p.Glu592=
XM_011544194.1:c.1944A>G	XP_011542496.1:p.Glu648=
XM_005273141.5:c.1773A>G	XP_005273198.1:p.Glu591=
XM_006711770.3:c.840A>G	XP_006711833.1:p.Glu280=
XM_011544194.3:c.1944A>G	XP_011542496.1:p.Glu648=
XM_017001329.2:c.1944A>G	XP_016856818.1:p.Glu648=
XM_017001330.2:c.1944A>G	XP_016856819.1:p.Glu648=
NM_001291940.2:c.555A>G	NP_001278869.1:p.Glu185=
NM_000254.3:c.1776A>G MANE Select	NP_000245.2:p.Glu592=