Canonical Allele Identifier: CA7451940

Gene: TRPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31028373G>A , CM000677.2:g.31028373G>A	GRCh38
NC_000015.9:g.31320576G>A , CM000677.1:g.31320576G>A	GRCh37
NC_000015.8:g.29107868G>A	NCBI36
NG_016453.1:g.78349C>T
NG_016453.2:g.137901C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001252024.2:c.3252C>T MANE Select	NP_001238953.1:p.Val1084=
ENST00000256552.11:c.3252C>T MANE Select	ENSP00000256552.7:p.Val1084=
NM_001252020.1:c.3303C>T	NP_001238949.1:p.Val1101=
NM_001252020.2:c.3303C>T	NP_001238949.1:p.Val1101=
NM_001252024.1:c.3252C>T	NP_001238953.1:p.Val1084=
NM_002420.5:c.3186C>T	NP_002411.3:p.Val1062=
NM_002420.6:c.3186C>T	NP_002411.3:p.Val1062=
ENST00000256552.10:c.3252C>T	ENSP00000256552.6:p.Val1084=
ENST00000397795.6:c.3186C>T	ENSP00000380897.2:p.Val1062=
ENST00000397795.7:c.3186C>T	ENSP00000380897.2:p.Val1062=
ENST00000542188.5:c.3303C>T	ENSP00000437849.1:p.Val1101=
ENST00000558212.5:n.475C>T
ENST00000558445.5:c.3186C>T	ENSP00000452946.1:p.Val1062=
ENST00000558445.6:c.3303C>T	ENSP00000452946.2:p.Val1101=
ENST00000558768.5:c.2955C>T	ENSP00000453119.2:p.Val985=
ENST00000559177.5:c.531C>T	ENSP00000453477.1:p.Val177=
ENST00000559177.6:c.648C>T	ENSP00000453477.2:p.Val216=
ENST00000560801.5:c.2828C>T	ENSP00000453644.2:n.2828C>T
ENST00000711434.1:c.3204C>T	ENSP00000518752.1:p.Val1068=
XR_001751769.1:n.278+1262G>A
XR_932055.1:n.260+1262G>A
XR_932056.1:n.89+1262G>A
XR_932057.1:n.260+1262G>A
XR_932058.1:n.88+1262G>A