Canonical Allele Identifier: CA345375062

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237016278G>T (hg19) ; chr1:g.236852978G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852978G>T , CM000663.2:g.236852978G>T	GRCh38
NC_000001.10:g.237016278G>T , CM000663.1:g.237016278G>T	GRCh37
NC_000001.9:g.235082901G>T	NCBI36
NG_008959.1:g.62698G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1843G>T MANE Select	ENSP00000355536.5:p.Gly615Ter
ENST00000535889.6:c.1843G>T	ENSP00000441845.1:p.Gly615Ter
ENST00000650888.1:c.*885G>T	ENSP00000498393.1:n.*885G>T
ENST00000651455.1:c.*587G>T	ENSP00000498963.1:n.*587G>T
ENST00000674797.2:c.1495G>T	ENSP00000502299.2:p.Gly499Ter
ENST00000679569.1:n.2157G>T
ENST00000679842.1:c.1843G>T	ENSP00000506109.1:p.Gly615Ter
ENST00000680454.1:n.2287G>T
ENST00000681102.1:c.1663G>T	ENSP00000505600.1:p.Gly555Ter
ENST00000681177.1:c.1516-6855G>T	ENSP00000506327.1:n.1516-6855G>T
ENST00000681937.1:n.2148-6855G>T
ENST00000366576.3:c.505G>T	ENSP00000355535.3:p.Gly169Ter
ENST00000366577.9:c.1843G>T	ENSP00000355536.5:p.Gly615Ter
ENST00000463959.1:n.1862G>T
ENST00000535889.5:c.1843G>T	ENSP00000441845.1:p.Gly615Ter
NM_000254.2:c.1843G>T	NP_000245.2:p.Gly615Ter
NM_001291939.1:c.1843G>T	NP_001278868.1:p.Gly615Ter
NM_001291940.1:c.622G>T	NP_001278869.1:p.Gly208Ter
XM_005273141.3:c.1840G>T	XP_005273198.1:p.Gly614Ter
XM_006711769.2:c.1843G>T	XP_006711832.1:p.Gly615Ter
XM_006711770.1:c.907G>T	XP_006711833.1:p.Gly303Ter
XM_011544193.1:c.1843G>T	XP_011542495.1:p.Gly615Ter
XM_011544194.1:c.2011G>T	XP_011542496.1:p.Gly671Ter
XM_005273141.5:c.1840G>T	XP_005273198.1:p.Gly614Ter
XM_006711770.3:c.907G>T	XP_006711833.1:p.Gly303Ter
XM_011544194.3:c.2011G>T	XP_011542496.1:p.Gly671Ter
XM_017001329.2:c.2011G>T	XP_016856818.1:p.Gly671Ter
XM_017001330.2:c.2011G>T	XP_016856819.1:p.Gly671Ter
NM_001291940.2:c.622G>T	NP_001278869.1:p.Gly208Ter
NM_000254.3:c.1843G>T MANE Select	NP_000245.2:p.Gly615Ter