Canonical Allele Identifier: CA345384397

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048438T>A (hg19) ; chr1:g.236885138T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885138T>A , CM000663.2:g.236885138T>A	GRCh38
NC_000001.10:g.237048438T>A , CM000663.1:g.237048438T>A	GRCh37
NC_000001.9:g.235115061T>A	NCBI36
NG_008959.1:g.94858T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2694T>A MANE Select	ENSP00000355536.5:p.Asp898Glu
ENST00000535889.6:c.2541T>A	ENSP00000441845.1:p.Asp847Glu
ENST00000650888.1:c.*1736T>A	ENSP00000498393.1:n.*1736T>A
ENST00000651455.1:c.*1438T>A	ENSP00000498963.1:n.*1438T>A
ENST00000674797.2:c.2346T>A	ENSP00000502299.2:p.Asp782Glu
ENST00000679569.1:n.3008T>A
ENST00000679842.1:c.2505T>A	ENSP00000506109.1:p.Asp835Glu
ENST00000680454.1:n.3138T>A
ENST00000681102.1:c.2514T>A	ENSP00000505600.1:p.Asp838Glu
ENST00000681177.1:c.2256T>A	ENSP00000506327.1:p.Asp752Glu
ENST00000681937.1:n.2888T>A
ENST00000366576.3:c.1356T>A	ENSP00000355535.3:p.Asp452Glu
ENST00000366577.9:c.2694T>A	ENSP00000355536.5:p.Asp898Glu
ENST00000535889.5:c.2541T>A	ENSP00000441845.1:p.Asp847Glu
NM_000254.2:c.2694T>A	NP_000245.2:p.Asp898Glu
NM_001291939.1:c.2541T>A	NP_001278868.1:p.Asp847Glu
NM_001291940.1:c.1473T>A	NP_001278869.1:p.Asp491Glu
XM_005273141.3:c.2691T>A	XP_005273198.1:p.Asp897Glu
XM_006711769.2:c.2694T>A	XP_006711832.1:p.Asp898Glu
XM_006711770.1:c.1758T>A	XP_006711833.1:p.Asp586Glu
XM_011544193.1:c.2505T>A	XP_011542495.1:p.Asp835Glu
XM_011544194.1:c.2862T>A	XP_011542496.1:p.Asp954Glu
XM_005273141.5:c.2691T>A	XP_005273198.1:p.Asp897Glu
XM_006711770.3:c.1758T>A	XP_006711833.1:p.Asp586Glu
XM_011544194.3:c.2862T>A	XP_011542496.1:p.Asp954Glu
XM_017001329.2:c.2709T>A	XP_016856818.1:p.Asp903Glu
XM_017001330.2:c.2673T>A	XP_016856819.1:p.Asp891Glu
NM_001291940.2:c.1473T>A	NP_001278869.1:p.Asp491Glu
NM_000254.3:c.2694T>A MANE Select	NP_000245.2:p.Asp898Glu