Canonical Allele Identifier: CA423816338

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048438T>C (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2694T>C MANE Select	ENSP00000355536.5:p.Asp898=
ENST00000535889.6:c.2541T>C	ENSP00000441845.1:p.Asp847=
ENST00000650888.1:c.*1736T>C	ENSP00000498393.1:n.*1736T>C
ENST00000651455.1:c.*1438T>C	ENSP00000498963.1:n.*1438T>C
ENST00000674797.2:c.2346T>C	ENSP00000502299.2:p.Asp782=
ENST00000679569.1:n.3008T>C
ENST00000679842.1:c.2505T>C	ENSP00000506109.1:p.Asp835=
ENST00000680454.1:n.3138T>C
ENST00000681102.1:c.2514T>C	ENSP00000505600.1:p.Asp838=
ENST00000681177.1:c.2256T>C	ENSP00000506327.1:p.Asp752=
ENST00000681937.1:n.2888T>C
ENST00000366576.3:c.1356T>C	ENSP00000355535.3:p.Asp452=
ENST00000366577.9:c.2694T>C	ENSP00000355536.5:p.Asp898=
ENST00000535889.5:c.2541T>C	ENSP00000441845.1:p.Asp847=
NM_000254.2:c.2694T>C	NP_000245.2:p.Asp898=
NM_001291939.1:c.2541T>C	NP_001278868.1:p.Asp847=
NM_001291940.1:c.1473T>C	NP_001278869.1:p.Asp491=
XM_005273141.3:c.2691T>C	XP_005273198.1:p.Asp897=
XM_006711769.2:c.2694T>C	XP_006711832.1:p.Asp898=
XM_006711770.1:c.1758T>C	XP_006711833.1:p.Asp586=
XM_011544193.1:c.2505T>C	XP_011542495.1:p.Asp835=
XM_011544194.1:c.2862T>C	XP_011542496.1:p.Asp954=
XM_005273141.5:c.2691T>C	XP_005273198.1:p.Asp897=
XM_006711770.3:c.1758T>C	XP_006711833.1:p.Asp586=
XM_011544194.3:c.2862T>C	XP_011542496.1:p.Asp954=
XM_017001329.2:c.2709T>C	XP_016856818.1:p.Asp903=
XM_017001330.2:c.2673T>C	XP_016856819.1:p.Asp891=
NM_001291940.2:c.1473T>C	NP_001278869.1:p.Asp491=
NM_000254.3:c.2694T>C MANE Select	NP_000245.2:p.Asp898=