Canonical Allele Identifier: CA345383336

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237044135T>A (hg19) ; chr1:g.236880835T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236880835T>A , CM000663.2:g.236880835T>A	GRCh38
NC_000001.10:g.237044135T>A , CM000663.1:g.237044135T>A	GRCh37
NC_000001.9:g.235110758T>A	NCBI36
NG_008959.1:g.90555T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2675T>A MANE Select	ENSP00000355536.5:p.Val892Glu
ENST00000535889.6:c.2522T>A	ENSP00000441845.1:p.Val841Glu
ENST00000650888.1:c.*1717T>A	ENSP00000498393.1:n.*1717T>A
ENST00000651455.1:c.*1419T>A	ENSP00000498963.1:n.*1419T>A
ENST00000674797.2:c.2327T>A	ENSP00000502299.2:p.Val776Glu
ENST00000679569.1:n.2989T>A
ENST00000679842.1:c.2486T>A	ENSP00000506109.1:p.Val829Glu
ENST00000680454.1:n.3119T>A
ENST00000681102.1:c.2495T>A	ENSP00000505600.1:p.Val832Glu
ENST00000681177.1:c.2237T>A	ENSP00000506327.1:p.Val746Glu
ENST00000681937.1:n.2869T>A
ENST00000366576.3:c.1337T>A	ENSP00000355535.3:p.Val446Glu
ENST00000366577.9:c.2675T>A	ENSP00000355536.5:p.Val892Glu
ENST00000535889.5:c.2522T>A	ENSP00000441845.1:p.Val841Glu
NM_000254.2:c.2675T>A	NP_000245.2:p.Val892Glu
NM_001291939.1:c.2522T>A	NP_001278868.1:p.Val841Glu
NM_001291940.1:c.1454T>A	NP_001278869.1:p.Val485Glu
XM_005273141.3:c.2672T>A	XP_005273198.1:p.Val891Glu
XM_006711769.2:c.2675T>A	XP_006711832.1:p.Val892Glu
XM_006711770.1:c.1739T>A	XP_006711833.1:p.Val580Glu
XM_011544193.1:c.2486T>A	XP_011542495.1:p.Val829Glu
XM_011544194.1:c.2843T>A	XP_011542496.1:p.Val948Glu
XM_005273141.5:c.2672T>A	XP_005273198.1:p.Val891Glu
XM_006711770.3:c.1739T>A	XP_006711833.1:p.Val580Glu
XM_011544194.3:c.2843T>A	XP_011542496.1:p.Val948Glu
XM_017001329.2:c.2690T>A	XP_016856818.1:p.Val897Glu
XM_017001330.2:c.2654T>A	XP_016856819.1:p.Val885Glu
NM_001291940.2:c.1454T>A	NP_001278869.1:p.Val485Glu
NM_000254.3:c.2675T>A MANE Select	NP_000245.2:p.Val892Glu