Canonical Allele Identifier: CA391537697

Gene: TRPM1

Linked Data

• MyVariant Identifiers: chr15:g.31362409G>C (hg19) ; chr15:g.31070206G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31070206G>C , CM000677.2:g.31070206G>C	GRCh38
NC_000015.9:g.31362409G>C , CM000677.1:g.31362409G>C	GRCh37
NC_000015.8:g.29149701G>C	NCBI36
NG_016453.1:g.36516C>G
NG_016453.2:g.96068C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711434.1:c.38C>G	ENSP00000518752.1:p.Thr13Ser
ENST00000397795.7:c.38C>G	ENSP00000380897.2:p.Thr13Ser
ENST00000558445.6:c.155C>G	ENSP00000452946.2:p.Thr52Ser
ENST00000559177.6:c.155C>G	ENSP00000453477.2:p.Thr52Ser
ENST00000559179.2:c.38C>G	ENSP00000453851.1:p.Thr13Ser
ENST00000256552.11:c.104C>G MANE Select	ENSP00000256552.7:p.Thr35Ser
ENST00000256552.10:c.104C>G	ENSP00000256552.6:p.Thr35Ser
ENST00000397795.6:c.38C>G	ENSP00000380897.2:p.Thr13Ser
ENST00000542188.5:c.155C>G	ENSP00000437849.1:p.Thr52Ser
ENST00000558445.5:c.38C>G	ENSP00000452946.1:p.Thr13Ser
ENST00000559177.5:c.38C>G	ENSP00000453477.1:p.Thr13Ser
ENST00000559179.1:c.38C>G	ENSP00000453851.1:p.Thr13Ser
ENST00000560658.5:c.38C>G	ENSP00000454077.1:p.Thr13Ser
NM_001252020.1:c.155C>G	NP_001238949.1:p.Thr52Ser
NM_001252024.1:c.104C>G	NP_001238953.1:p.Thr35Ser
NM_001252030.1:c.38C>G	NP_001238959.1:p.Thr13Ser
NM_002420.5:c.38C>G	NP_002411.3:p.Thr13Ser
NM_001252024.2:c.104C>G MANE Select	NP_001238953.1:p.Thr35Ser
NM_001252030.2:c.38C>G	NP_001238959.1:p.Thr13Ser
NM_002420.6:c.38C>G	NP_002411.3:p.Thr13Ser
NM_001252020.2:c.155C>G	NP_001238949.1:p.Thr52Ser