Canonical Allele Identifier: CA7453123

Gene: TRPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31076904C>T , CM000677.2:g.31076904C>T	GRCh38
NC_000015.9:g.31369107C>T , CM000677.1:g.31369107C>T	GRCh37
NC_000015.8:g.29156399C>T	NCBI36
NG_016453.1:g.29818G>A
NG_016453.2:g.89370G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001252024.2:c.83+1G>A MANE Select	NP_001238953.1:n.83+1G>A
ENST00000256552.11:c.83+1G>A MANE Select	ENSP00000256552.7:n.83+1G>A
NM_001252020.1:c.134+1G>A	NP_001238949.1:n.134+1G>A
NM_001252020.2:c.134+1G>A	NP_001238949.1:n.134+1G>A
NM_001252024.1:c.83+1G>A	NP_001238953.1:n.83+1G>A
NM_001252030.1:c.17+1G>A	NP_001238959.1:n.17+1G>A
NM_001252030.2:c.17+1G>A	NP_001238959.1:n.17+1G>A
NM_002420.5:c.17+1G>A	NP_002411.3:n.17+1G>A
NM_002420.6:c.17+1G>A	NP_002411.3:n.17+1G>A
ENST00000256552.10:c.83+1G>A	ENSP00000256552.6:n.83+1G>A
ENST00000397795.6:c.17+1G>A	ENSP00000380897.2:n.17+1G>A
ENST00000397795.7:c.17+1G>A	ENSP00000380897.2:n.17+1G>A
ENST00000542188.5:c.134+1G>A	ENSP00000437849.1:n.134+1G>A
ENST00000558445.5:c.17+1G>A	ENSP00000452946.1:n.17+1G>A
ENST00000558445.6:c.134+1G>A	ENSP00000452946.2:n.134+1G>A
ENST00000559177.5:c.17+1G>A	ENSP00000453477.1:n.17+1G>A
ENST00000559177.6:c.134+1G>A	ENSP00000453477.2:n.134+1G>A
ENST00000559179.1:c.17+1G>A	ENSP00000453851.1:n.17+1G>A
ENST00000559179.2:c.17+1G>A	ENSP00000453851.1:n.17+1G>A
ENST00000560658.5:c.17+1G>A	ENSP00000454077.1:n.17+1G>A
ENST00000711434.1:c.17+1G>A	ENSP00000518752.1:n.17+1G>A