Canonical Allele Identifier: CA7451641

Gene: TRPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31002248C>T , CM000677.2:g.31002248C>T	GRCh38
NC_000015.9:g.31294451C>T , CM000677.1:g.31294451C>T	GRCh37
NC_000015.8:g.29081743C>T	NCBI36
NG_016453.1:g.104474G>A
NG_016453.2:g.164026G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711434.1:c.4404G>A	ENSP00000518752.1:p.Thr1468=
ENST00000397795.7:c.4386G>A	ENSP00000380897.2:p.Thr1462=
ENST00000558445.6:c.4503G>A	ENSP00000452946.2:p.Thr1501=
ENST00000559177.6:c.1848G>A	ENSP00000453477.2:p.Thr616=
ENST00000256552.11:c.4452G>A MANE Select	ENSP00000256552.7:p.Thr1484=
ENST00000256552.10:c.4452G>A	ENSP00000256552.6:p.Thr1484=
ENST00000397795.6:c.4386G>A	ENSP00000380897.2:p.Thr1462=
ENST00000542188.5:c.4503G>A	ENSP00000437849.1:p.Thr1501=
ENST00000558768.5:c.4155G>A	ENSP00000453119.2:p.Thr1385=
ENST00000560801.5:c.4028G>A	ENSP00000453644.2:n.4028G>A
NM_001252020.1:c.4503G>A	NP_001238949.1:p.Thr1501=
NM_001252024.1:c.4452G>A	NP_001238953.1:p.Thr1484=
NM_002420.5:c.4386G>A	NP_002411.3:p.Thr1462=
NM_001252024.2:c.4452G>A MANE Select	NP_001238953.1:p.Thr1484=
NM_002420.6:c.4386G>A	NP_002411.3:p.Thr1462=
NM_001252020.2:c.4503G>A	NP_001238949.1:p.Thr1501=