Canonical Allele Identifier: CA7453125
Community Standard Title: NM_001252024.2(TRPM1):c.75C>T (p.Asp25=)
Gene: TRPM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.31076913G>A , CM000677.2:g.31076913G>A GRCh38
NC_000015.9:g.31369116G>A , CM000677.1:g.31369116G>A GRCh37
NC_000015.8:g.29156408G>A NCBI36
NG_016453.1:g.29809C>T
NG_016453.2:g.89361C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001252024.2:c.75C>T MANE Select NP_001238953.1:p.Asp25=
ENST00000256552.11:c.75C>T MANE Select ENSP00000256552.7:p.Asp25=
NM_001252020.1:c.126C>T NP_001238949.1:p.Asp42=
NM_001252020.2:c.126C>T NP_001238949.1:p.Asp42=
NM_001252024.1:c.75C>T NP_001238953.1:p.Asp25=
NM_001252030.1:c.9C>T NP_001238959.1:p.Asp3=
NM_001252030.2:c.9C>T NP_001238959.1:p.Asp3=
NM_002420.5:c.9C>T NP_002411.3:p.Asp3=
NM_002420.6:c.9C>T NP_002411.3:p.Asp3=
ENST00000256552.10:c.75C>T ENSP00000256552.6:p.Asp25=
ENST00000397795.6:c.9C>T ENSP00000380897.2:p.Asp3=
ENST00000397795.7:c.9C>T ENSP00000380897.2:p.Asp3=
ENST00000542188.5:c.126C>T ENSP00000437849.1:p.Asp42=
ENST00000558445.5:c.9C>T ENSP00000452946.1:p.Asp3=
ENST00000558445.6:c.126C>T ENSP00000452946.2:p.Asp42=
ENST00000559177.5:c.9C>T ENSP00000453477.1:p.Asp3=
ENST00000559177.6:c.126C>T ENSP00000453477.2:p.Asp42=
ENST00000559179.1:c.9C>T ENSP00000453851.1:p.Asp3=
ENST00000559179.2:c.9C>T ENSP00000453851.1:p.Asp3=
ENST00000560658.5:c.9C>T ENSP00000454077.1:p.Asp3=
ENST00000711434.1:c.9C>T ENSP00000518752.1:p.Asp3=