Canonical Allele Identifier: CA489644906

Gene: TRPM1

Linked Data

• gnomAD v4: 15-31070133-A-C
• MyVariant Identifiers: chr15:g.31362336A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31070133A>C , CM000677.2:g.31070133A>C	GRCh38
NC_000015.9:g.31362336A>C , CM000677.1:g.31362336A>C	GRCh37
NC_000015.8:g.29149628A>C	NCBI36
NG_016453.1:g.36589T>G
NG_016453.2:g.96141T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711434.1:c.111T>G	ENSP00000518752.1:p.Thr37=
ENST00000397795.7:c.111T>G	ENSP00000380897.2:p.Thr37=
ENST00000558445.6:c.228T>G	ENSP00000452946.2:p.Thr76=
ENST00000559177.6:c.228T>G	ENSP00000453477.2:p.Thr76=
ENST00000559179.2:c.111T>G	ENSP00000453851.1:p.Thr37=
ENST00000256552.11:c.177T>G MANE Select	ENSP00000256552.7:p.Thr59=
ENST00000256552.10:c.177T>G	ENSP00000256552.6:p.Thr59=
ENST00000397795.6:c.111T>G	ENSP00000380897.2:p.Thr37=
ENST00000542188.5:c.228T>G	ENSP00000437849.1:p.Thr76=
ENST00000558445.5:c.111T>G	ENSP00000452946.1:p.Thr37=
ENST00000559177.5:c.111T>G	ENSP00000453477.1:p.Thr37=
ENST00000559179.1:c.111T>G	ENSP00000453851.1:p.Thr37=
ENST00000560658.5:c.111T>G	ENSP00000454077.1:p.Thr37=
NM_001252020.1:c.228T>G	NP_001238949.1:p.Thr76=
NM_001252024.1:c.177T>G	NP_001238953.1:p.Thr59=
NM_001252030.1:c.111T>G	NP_001238959.1:p.Thr37=
NM_002420.5:c.111T>G	NP_002411.3:p.Thr37=
NM_001252024.2:c.177T>G MANE Select	NP_001238953.1:p.Thr59=
NM_001252030.2:c.111T>G	NP_001238959.1:p.Thr37=
NM_002420.6:c.111T>G	NP_002411.3:p.Thr37=
NM_001252020.2:c.228T>G	NP_001238949.1:p.Thr76=