Canonical Allele Identifier: CA1144555713

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852605A= , CM000663.2:g.236852605A=	GRCh38
NC_000001.10:g.237015905A= , CM000663.1:g.237015905A=	GRCh37
NC_000001.9:g.235082528A=	NCBI36
NG_008959.1:g.62325A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1780A= MANE Select	ENSP00000355536.5:p.Met594=
ENST00000535889.6:c.1780A=	ENSP00000441845.1:p.Met594=
ENST00000650888.1:c.*822A=	ENSP00000498393.1:n.*822A=
ENST00000651455.1:c.*524A=	ENSP00000498963.1:n.*524A=
ENST00000674797.2:c.1432A=	ENSP00000502299.2:p.Met478=
ENST00000679569.1:n.2094A=
ENST00000679842.1:c.1780A=	ENSP00000506109.1:p.Met594=
ENST00000680454.1:n.2224A=
ENST00000681102.1:c.1600A=	ENSP00000505600.1:p.Met534=
ENST00000681177.1:c.1516-7228A=	ENSP00000506327.1:n.1516-7228A=
ENST00000681937.1:n.2148-7228A=
ENST00000366576.3:c.442A=	ENSP00000355535.3:p.Met148=
ENST00000366577.9:c.1780A=	ENSP00000355536.5:p.Met594=
ENST00000463959.1:n.1799A=
ENST00000535889.5:c.1780A=	ENSP00000441845.1:p.Met594=
NM_000254.2:c.1780A=	NP_000245.2:p.Met594=
NM_001291939.1:c.1780A=	NP_001278868.1:p.Met594=
NM_001291940.1:c.559A=	NP_001278869.1:p.Met187=
XM_005273141.3:c.1777A=	XP_005273198.1:p.Met593=
XM_006711769.2:c.1780A=	XP_006711832.1:p.Met594=
XM_006711770.1:c.844A=	XP_006711833.1:p.Met282=
XM_011544193.1:c.1780A=	XP_011542495.1:p.Met594=
XM_011544194.1:c.1948A=	XP_011542496.1:p.Met650=
XM_005273141.5:c.1777A=	XP_005273198.1:p.Met593=
XM_006711770.3:c.844A=	XP_006711833.1:p.Met282=
XM_011544194.3:c.1948A=	XP_011542496.1:p.Met650=
XM_017001329.2:c.1948A=	XP_016856818.1:p.Met650=
XM_017001330.2:c.1948A=	XP_016856819.1:p.Met650=
NM_001291940.2:c.559A=	NP_001278869.1:p.Met187=
NM_000254.3:c.1780A= MANE Select	NP_000245.2:p.Met594=