Canonical Allele Identifier: CA345375067

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237016279G>T (hg19) ; chr1:g.236852979G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852979G>T , CM000663.2:g.236852979G>T	GRCh38
NC_000001.10:g.237016279G>T , CM000663.1:g.237016279G>T	GRCh37
NC_000001.9:g.235082902G>T	NCBI36
NG_008959.1:g.62699G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1844G>T MANE Select	ENSP00000355536.5:p.Gly615Val
ENST00000535889.6:c.1844G>T	ENSP00000441845.1:p.Gly615Val
ENST00000650888.1:c.*886G>T	ENSP00000498393.1:n.*886G>T
ENST00000651455.1:c.*588G>T	ENSP00000498963.1:n.*588G>T
ENST00000674797.2:c.1496G>T	ENSP00000502299.2:p.Gly499Val
ENST00000679569.1:n.2158G>T
ENST00000679842.1:c.1844G>T	ENSP00000506109.1:p.Gly615Val
ENST00000680454.1:n.2288G>T
ENST00000681102.1:c.1664G>T	ENSP00000505600.1:p.Gly555Val
ENST00000681177.1:c.1516-6854G>T	ENSP00000506327.1:n.1516-6854G>T
ENST00000681937.1:n.2148-6854G>T
ENST00000366576.3:c.506G>T	ENSP00000355535.3:p.Gly169Val
ENST00000366577.9:c.1844G>T	ENSP00000355536.5:p.Gly615Val
ENST00000463959.1:n.1863G>T
ENST00000535889.5:c.1844G>T	ENSP00000441845.1:p.Gly615Val
NM_000254.2:c.1844G>T	NP_000245.2:p.Gly615Val
NM_001291939.1:c.1844G>T	NP_001278868.1:p.Gly615Val
NM_001291940.1:c.623G>T	NP_001278869.1:p.Gly208Val
XM_005273141.3:c.1841G>T	XP_005273198.1:p.Gly614Val
XM_006711769.2:c.1844G>T	XP_006711832.1:p.Gly615Val
XM_006711770.1:c.908G>T	XP_006711833.1:p.Gly303Val
XM_011544193.1:c.1844G>T	XP_011542495.1:p.Gly615Val
XM_011544194.1:c.2012G>T	XP_011542496.1:p.Gly671Val
XM_005273141.5:c.1841G>T	XP_005273198.1:p.Gly614Val
XM_006711770.3:c.908G>T	XP_006711833.1:p.Gly303Val
XM_011544194.3:c.2012G>T	XP_011542496.1:p.Gly671Val
XM_017001329.2:c.2012G>T	XP_016856818.1:p.Gly671Val
XM_017001330.2:c.2012G>T	XP_016856819.1:p.Gly671Val
NM_001291940.2:c.623G>T	NP_001278869.1:p.Gly208Val
NM_000254.3:c.1844G>T MANE Select	NP_000245.2:p.Gly615Val