Canonical Allele Identifier: CA2167784165

Gene: TRPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31070141C= , CM000677.2:g.31070141C=	GRCh38
NC_000015.9:g.31362344C= , CM000677.1:g.31362344C=	GRCh37
NC_000015.8:g.29149636C=	NCBI36
NG_016453.1:g.36581G=
NG_016453.2:g.96133G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711434.1:c.103G=	ENSP00000518752.1:p.Val35=
ENST00000397795.7:c.103G=	ENSP00000380897.2:p.Val35=
ENST00000558445.6:c.220G=	ENSP00000452946.2:p.Val74=
ENST00000559177.6:c.220G=	ENSP00000453477.2:p.Val74=
ENST00000559179.2:c.103G=	ENSP00000453851.1:p.Val35=
ENST00000256552.11:c.169G= MANE Select	ENSP00000256552.7:p.Val57=
ENST00000256552.10:c.169G=	ENSP00000256552.6:p.Val57=
ENST00000397795.6:c.103G=	ENSP00000380897.2:p.Val35=
ENST00000542188.5:c.220G=	ENSP00000437849.1:p.Val74=
ENST00000558445.5:c.103G=	ENSP00000452946.1:p.Val35=
ENST00000559177.5:c.103G=	ENSP00000453477.1:p.Val35=
ENST00000559179.1:c.103G=	ENSP00000453851.1:p.Val35=
ENST00000560658.5:c.103G=	ENSP00000454077.1:p.Val35=
NM_001252020.1:c.220G=	NP_001238949.1:p.Val74=
NM_001252024.1:c.169G=	NP_001238953.1:p.Val57=
NM_001252030.1:c.103G=	NP_001238959.1:p.Val35=
NM_002420.5:c.103G=	NP_002411.3:p.Val35=
NM_001252024.2:c.169G= MANE Select	NP_001238953.1:p.Val57=
NM_001252030.2:c.103G=	NP_001238959.1:p.Val35=
NM_002420.6:c.103G=	NP_002411.3:p.Val35=
NM_001252020.2:c.220G=	NP_001238949.1:p.Val74=