Canonical Allele Identifier: CA201886
Gene: TRPM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.31031046G>A , CM000677.2:g.31031046G>A GRCh38
NC_000015.9:g.31323249G>A , CM000677.1:g.31323249G>A GRCh37
NC_000015.8:g.29110541G>A NCBI36
NG_016453.1:g.75676C>T
NG_016453.2:g.135228C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000711434.1:c.2998C>T ENSP00000518752.1:p.Arg1000Ter
ENST00000397795.7:c.2998C>T ENSP00000380897.2:p.Arg1000Ter
ENST00000558445.6:c.3115C>T ENSP00000452946.2:p.Arg1039Ter
ENST00000559177.6:c.545-2570C>T ENSP00000453477.2:n.545-2570C>T
ENST00000256552.11:c.3064C>T MANE Select ENSP00000256552.7:p.Arg1022Ter
ENST00000256552.10:c.3064C>T ENSP00000256552.6:p.Arg1022Ter
ENST00000397795.6:c.2998C>T ENSP00000380897.2:p.Arg1000Ter
ENST00000542188.5:c.3115C>T ENSP00000437849.1:p.Arg1039Ter
ENST00000557948.1:n.439C>T
ENST00000558212.5:n.287C>T
ENST00000558445.5:c.2998C>T ENSP00000452946.1:p.Arg1000Ter
ENST00000558768.5:c.2767C>T ENSP00000453119.2:p.Arg923Ter
ENST00000559177.5:c.428-2570C>T ENSP00000453477.1:n.428-2570C>T
ENST00000560801.5:c.2703+1643C>T ENSP00000453644.2:n.2703+1643C>T
NM_001252020.1:c.3115C>T NP_001238949.1:p.Arg1039Ter
NM_001252024.1:c.3064C>T NP_001238953.1:p.Arg1022Ter
NM_002420.5:c.2998C>T NP_002411.3:p.Arg1000Ter
XR_932055.1:n.260+3935G>A
XR_932056.1:n.89+3935G>A
XR_932057.1:n.260+3935G>A
XR_932058.1:n.88+3935G>A
XR_001751769.1:n.278+3935G>A
NM_001252024.2:c.3064C>T MANE Select NP_001238953.1:p.Arg1022Ter
NM_002420.6:c.2998C>T NP_002411.3:p.Arg1000Ter
NM_001252020.2:c.3115C>T NP_001238949.1:p.Arg1039Ter