Canonical Allele Identifier: CA7452760
Gene: TRPM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.31063118C>T , CM000677.2:g.31063118C>T GRCh38
NC_000015.9:g.31355321C>T , CM000677.1:g.31355321C>T GRCh37
NC_000015.8:g.29142613C>T NCBI36
NG_016453.1:g.43604G>A
NG_016453.2:g.103156G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000711434.1:c.899G>A ENSP00000518752.1:p.Gly300Glu
ENST00000397795.7:c.899G>A ENSP00000380897.2:p.Gly300Glu
ENST00000558445.6:c.1016G>A ENSP00000452946.2:p.Gly339Glu
ENST00000559177.6:c.544+4761G>A ENSP00000453477.2:n.544+4761G>A
ENST00000256552.11:c.965G>A MANE Select ENSP00000256552.7:p.Gly322Glu
ENST00000256552.10:c.965G>A ENSP00000256552.6:p.Gly322Glu
ENST00000397795.6:c.899G>A ENSP00000380897.2:p.Gly300Glu
ENST00000542188.5:c.1016G>A ENSP00000437849.1:p.Gly339Glu
ENST00000558445.5:c.899G>A ENSP00000452946.1:p.Gly300Glu
ENST00000558768.5:c.668+18G>A ENSP00000453119.2:n.668+18G>A
ENST00000559177.5:c.427+4761G>A ENSP00000453477.1:n.427+4761G>A
ENST00000560658.5:c.899G>A ENSP00000454077.1:p.Gly300Glu
ENST00000560801.5:c.686G>A ENSP00000453644.2:p.Gly229Glu
NM_001252020.1:c.1016G>A NP_001238949.1:p.Gly339Glu
NM_001252024.1:c.965G>A NP_001238953.1:p.Gly322Glu
NM_002420.5:c.899G>A NP_002411.3:p.Gly300Glu
NM_001252024.2:c.965G>A MANE Select NP_001238953.1:p.Gly322Glu
NM_002420.6:c.899G>A NP_002411.3:p.Gly300Glu
NM_001252020.2:c.1016G>A NP_001238949.1:p.Gly339Glu