Canonical Allele Identifier: CA1474753

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236896996C>A , CM000663.2:g.236896996C>A	GRCh38
NC_000001.10:g.237060296C>A , CM000663.1:g.237060296C>A	GRCh37
NC_000001.9:g.235126919C>A	NCBI36
NG_008959.1:g.106716C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.3599-10C>A MANE Select	ENSP00000355536.5:n.3599-10C>A
ENST00000470570.2:n.4329-10C>A
ENST00000535889.6:c.3446-10C>A	ENSP00000441845.1:n.3446-10C>A
ENST00000650888.1:c.*2641-10C>A	ENSP00000498393.1:n.*2641-10C>A
ENST00000651455.1:c.*2343-10C>A	ENSP00000498963.1:n.*2343-10C>A
ENST00000674797.2:c.3251-10C>A	ENSP00000502299.2:n.3251-10C>A
ENST00000679569.1:n.6726-10C>A
ENST00000679842.1:c.3410-10C>A	ENSP00000506109.1:n.3410-10C>A
ENST00000680454.1:n.6856-10C>A
ENST00000681102.1:c.3419-10C>A	ENSP00000505600.1:n.3419-10C>A
ENST00000681177.1:c.3161-10C>A	ENSP00000506327.1:n.3161-10C>A
ENST00000681937.1:n.3793-10C>A
ENST00000366576.3:c.2261-10C>A	ENSP00000355535.3:n.2261-10C>A
ENST00000366577.9:c.3599-10C>A	ENSP00000355536.5:n.3599-10C>A
ENST00000470570.1:n.1211-10C>A
ENST00000535889.5:c.3446-10C>A	ENSP00000441845.1:n.3446-10C>A
NM_000254.2:c.3599-10C>A	NP_000245.2:n.3599-10C>A
NM_001291939.1:c.3446-10C>A	NP_001278868.1:n.3446-10C>A
NM_001291940.1:c.2378-10C>A	NP_001278869.1:n.2378-10C>A
XM_005273141.3:c.3596-10C>A	XP_005273198.1:n.3596-10C>A
XM_006711770.1:c.2663-10C>A	XP_006711833.1:n.2663-10C>A
XM_011544193.1:c.3410-10C>A	XP_011542495.1:n.3410-10C>A
XM_011544194.1:c.3767-10C>A	XP_011542496.1:n.3767-10C>A
XM_005273141.5:c.3596-10C>A	XP_005273198.1:n.3596-10C>A
XM_006711770.3:c.2663-10C>A	XP_006711833.1:n.2663-10C>A
XM_011544194.3:c.3767-10C>A	XP_011542496.1:n.3767-10C>A
XM_017001329.2:c.3614-10C>A	XP_016856818.1:n.3614-10C>A
XM_017001330.2:c.3578-10C>A	XP_016856819.1:n.3578-10C>A
NM_001291940.2:c.2378-10C>A	NP_001278869.1:n.2378-10C>A
NM_000254.3:c.3599-10C>A MANE Select	NP_000245.2:n.3599-10C>A