Canonical Allele Identifier: CA489644964
Gene: TRPM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.31362417G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.31070214G>C , CM000677.2:g.31070214G>C GRCh38
NC_000015.9:g.31362417G>C , CM000677.1:g.31362417G>C GRCh37
NC_000015.8:g.29149709G>C NCBI36
NG_016453.1:g.36508C>G
NG_016453.2:g.96060C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000711434.1:c.30C>G ENSP00000518752.1:p.Gly10=
ENST00000397795.7:c.30C>G ENSP00000380897.2:p.Gly10=
ENST00000558445.6:c.147C>G ENSP00000452946.2:p.Gly49=
ENST00000559177.6:c.147C>G ENSP00000453477.2:p.Gly49=
ENST00000559179.2:c.30C>G ENSP00000453851.1:p.Gly10=
ENST00000256552.11:c.96C>G MANE Select ENSP00000256552.7:p.Gly32=
ENST00000256552.10:c.96C>G ENSP00000256552.6:p.Gly32=
ENST00000397795.6:c.30C>G ENSP00000380897.2:p.Gly10=
ENST00000542188.5:c.147C>G ENSP00000437849.1:p.Gly49=
ENST00000558445.5:c.30C>G ENSP00000452946.1:p.Gly10=
ENST00000559177.5:c.30C>G ENSP00000453477.1:p.Gly10=
ENST00000559179.1:c.30C>G ENSP00000453851.1:p.Gly10=
ENST00000560658.5:c.30C>G ENSP00000454077.1:p.Gly10=
NM_001252020.1:c.147C>G NP_001238949.1:p.Gly49=
NM_001252024.1:c.96C>G NP_001238953.1:p.Gly32=
NM_001252030.1:c.30C>G NP_001238959.1:p.Gly10=
NM_002420.5:c.30C>G NP_002411.3:p.Gly10=
NM_001252024.2:c.96C>G MANE Select NP_001238953.1:p.Gly32=
NM_001252030.2:c.30C>G NP_001238959.1:p.Gly10=
NM_002420.6:c.30C>G NP_002411.3:p.Gly10=
NM_001252020.2:c.147C>G NP_001238949.1:p.Gly49=