Canonical Allele Identifier: CA7453080

Gene: TRPM1

Linked Data

• ClinVar Variation Id: 1433392
• ClinVar RCV Id: RCV001944411
• dbSNP Id: rs751427833
• ExAC: 15:31362432 G / C
• gnomAD v2: 15-31362432-G-C
• gnomAD v3: 15-31070229-G-C
• gnomAD v4: 15-31070229-G-C
• MyVariant Identifiers: chr15:g.31362432G>C (hg19) ; chr15:g.31070229G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31070229G>C , CM000677.2:g.31070229G>C	GRCh38
NC_000015.9:g.31362432G>C , CM000677.1:g.31362432G>C	GRCh37
NC_000015.8:g.29149724G>C	NCBI36
NG_016453.1:g.36493C>G
NG_016453.2:g.96045C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711434.1:c.18-3C>G	ENSP00000518752.1:n.18-3C>G
ENST00000397795.7:c.18-3C>G	ENSP00000380897.2:n.18-3C>G
ENST00000558445.6:c.135-3C>G	ENSP00000452946.2:n.135-3C>G
ENST00000559177.6:c.135-3C>G	ENSP00000453477.2:n.135-3C>G
ENST00000559179.2:c.18-3C>G	ENSP00000453851.1:n.18-3C>G
ENST00000256552.11:c.84-3C>G MANE Select	ENSP00000256552.7:n.84-3C>G
ENST00000256552.10:c.84-3C>G	ENSP00000256552.6:n.84-3C>G
ENST00000397795.6:c.18-3C>G	ENSP00000380897.2:n.18-3C>G
ENST00000542188.5:c.135-3C>G	ENSP00000437849.1:n.135-3C>G
ENST00000558445.5:c.18-3C>G	ENSP00000452946.1:n.18-3C>G
ENST00000559177.5:c.18-3C>G	ENSP00000453477.1:n.18-3C>G
ENST00000559179.1:c.18-3C>G	ENSP00000453851.1:n.18-3C>G
ENST00000560658.5:c.18-3C>G	ENSP00000454077.1:n.18-3C>G
NM_001252020.1:c.135-3C>G	NP_001238949.1:n.135-3C>G
NM_001252024.1:c.84-3C>G	NP_001238953.1:n.84-3C>G
NM_001252030.1:c.18-3C>G	NP_001238959.1:n.18-3C>G
NM_002420.5:c.18-3C>G	NP_002411.3:n.18-3C>G
NM_001252024.2:c.84-3C>G MANE Select	NP_001238953.1:n.84-3C>G
NM_001252030.2:c.18-3C>G	NP_001238959.1:n.18-3C>G
NM_002420.6:c.18-3C>G	NP_002411.3:n.18-3C>G
NM_001252020.2:c.135-3C>G	NP_001238949.1:n.135-3C>G