Canonical Allele Identifier: CA2167784168
Gene: TRPM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.31070148_31070149delinsGC , CM000677.2:g.31070148_31070149delinsGC GRCh38
NC_000015.9:g.31362351_31362352delinsGC , CM000677.1:g.31362351_31362352delinsGC GRCh37
NC_000015.8:g.29149643_29149644delinsGC NCBI36
NG_016453.1:g.36573_36574delinsGC
NG_016453.2:g.96125_96126delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000711434.1:c.95_96delinsGC ENSP00000518752.1:p.Ser32=
ENST00000397795.7:c.95_96delinsGC ENSP00000380897.2:p.Ser32=
ENST00000558445.6:c.212_213delinsGC ENSP00000452946.2:p.Ser71=
ENST00000559177.6:c.212_213delinsGC ENSP00000453477.2:p.Ser71=
ENST00000559179.2:c.95_96delinsGC ENSP00000453851.1:p.Ser32=
ENST00000256552.11:c.161_162delinsGC MANE Select ENSP00000256552.7:p.Ser54=
ENST00000256552.10:c.161_162delinsGC ENSP00000256552.6:p.Ser54=
ENST00000397795.6:c.95_96delinsGC ENSP00000380897.2:p.Ser32=
ENST00000542188.5:c.212_213delinsGC ENSP00000437849.1:p.Ser71=
ENST00000558445.5:c.95_96delinsGC ENSP00000452946.1:p.Ser32=
ENST00000559177.5:c.95_96delinsGC ENSP00000453477.1:p.Ser32=
ENST00000559179.1:c.95_96delinsGC ENSP00000453851.1:p.Ser32=
ENST00000560658.5:c.95_96delinsGC ENSP00000454077.1:p.Ser32=
NM_001252020.1:c.212_213delinsGC NP_001238949.1:p.Ser71=
NM_001252024.1:c.161_162delinsGC NP_001238953.1:p.Ser54=
NM_001252030.1:c.95_96delinsGC NP_001238959.1:p.Ser32=
NM_002420.5:c.95_96delinsGC NP_002411.3:p.Ser32=
NM_001252024.2:c.161_162delinsGC MANE Select NP_001238953.1:p.Ser54=
NM_001252030.2:c.95_96delinsGC NP_001238959.1:p.Ser32=
NM_002420.6:c.95_96delinsGC NP_002411.3:p.Ser32=
NM_001252020.2:c.212_213delinsGC NP_001238949.1:p.Ser71=