Canonical Allele Identifier: CA7451619

Gene: TRPM1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.31002140A>T , CM000677.2:g.31002140A>T	GRCh38
NC_000015.9:g.31294343A>T , CM000677.1:g.31294343A>T	GRCh37
NC_000015.8:g.29081635A>T	NCBI36
NG_016453.1:g.104582T>A
NG_016453.2:g.164134T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000711434.1:c.4512T>A	ENSP00000518752.1:p.His1504Gln
ENST00000397795.7:c.4494T>A	ENSP00000380897.2:p.His1498Gln
ENST00000558445.6:c.4611T>A	ENSP00000452946.2:p.His1537Gln
ENST00000559177.6:c.1956T>A	ENSP00000453477.2:p.His652Gln
ENST00000256552.11:c.4560T>A MANE Select	ENSP00000256552.7:p.His1520Gln
ENST00000256552.10:c.4560T>A	ENSP00000256552.6:p.His1520Gln
ENST00000397795.6:c.4494T>A	ENSP00000380897.2:p.His1498Gln
ENST00000542188.5:c.4611T>A	ENSP00000437849.1:p.His1537Gln
ENST00000558768.5:c.4263T>A	ENSP00000453119.2:p.His1421Gln
ENST00000560801.5:c.4136T>A	ENSP00000453644.2:n.4136T>A
NM_001252020.1:c.4611T>A	NP_001238949.1:p.His1537Gln
NM_001252024.1:c.4560T>A	NP_001238953.1:p.His1520Gln
NM_002420.5:c.4494T>A	NP_002411.3:p.His1498Gln
NM_001252024.2:c.4560T>A MANE Select	NP_001238953.1:p.His1520Gln
NM_002420.6:c.4494T>A	NP_002411.3:p.His1498Gln
NM_001252020.2:c.4611T>A	NP_001238949.1:p.His1537Gln