Canonical Allele Identifier: CA391537735
Gene: TRPM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.31070210A>C , CM000677.2:g.31070210A>C GRCh38
NC_000015.9:g.31362413A>C , CM000677.1:g.31362413A>C GRCh37
NC_000015.8:g.29149705A>C NCBI36
NG_016453.1:g.36512T>G
NG_016453.2:g.96064T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000711434.1:c.34T>G ENSP00000518752.1:p.Phe12Val
ENST00000397795.7:c.34T>G ENSP00000380897.2:p.Phe12Val
ENST00000558445.6:c.151T>G ENSP00000452946.2:p.Phe51Val
ENST00000559177.6:c.151T>G ENSP00000453477.2:p.Phe51Val
ENST00000559179.2:c.34T>G ENSP00000453851.1:p.Phe12Val
ENST00000256552.11:c.100T>G MANE Select ENSP00000256552.7:p.Phe34Val
ENST00000256552.10:c.100T>G ENSP00000256552.6:p.Phe34Val
ENST00000397795.6:c.34T>G ENSP00000380897.2:p.Phe12Val
ENST00000542188.5:c.151T>G ENSP00000437849.1:p.Phe51Val
ENST00000558445.5:c.34T>G ENSP00000452946.1:p.Phe12Val
ENST00000559177.5:c.34T>G ENSP00000453477.1:p.Phe12Val
ENST00000559179.1:c.34T>G ENSP00000453851.1:p.Phe12Val
ENST00000560658.5:c.34T>G ENSP00000454077.1:p.Phe12Val
NM_001252020.1:c.151T>G NP_001238949.1:p.Phe51Val
NM_001252024.1:c.100T>G NP_001238953.1:p.Phe34Val
NM_001252030.1:c.34T>G NP_001238959.1:p.Phe12Val
NM_002420.5:c.34T>G NP_002411.3:p.Phe12Val
NM_001252024.2:c.100T>G MANE Select NP_001238953.1:p.Phe34Val
NM_001252030.2:c.34T>G NP_001238959.1:p.Phe12Val
NM_002420.6:c.34T>G NP_002411.3:p.Phe12Val
NM_001252020.2:c.151T>G NP_001238949.1:p.Phe51Val