Canonical Allele Identifier: CA2627517272
Gene: TRPM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.31070241_31070242insCCCATGTTCGTAATAGATATTGTTCTAT , CM000677.2:g.31070241_31070242insCCCATGTTCGTAATAGATATTGTTCTAT GRCh38
NC_000015.9:g.31362444_31362445insCCCATGTTCGTAATAGATATTGTTCTAT , CM000677.1:g.31362444_31362445insCCCATGTTCGTAATAGATATTGTTCTAT GRCh37
NC_000015.8:g.29149736_29149737insCCCATGTTCGTAATAGATATTGTTCTAT NCBI36
NG_016453.1:g.36480_36481insATAGAACAATATCTATTACGAACATGGG
NG_016453.2:g.96032_96033insATAGAACAATATCTATTACGAACATGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000711434.1:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG ENSP00000518752.1:n.18-16_18-15insATAGAACAATATCTATTACGAACATGG...
ENST00000397795.7:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG ENSP00000380897.2:n.18-16_18-15insATAGAACAATATCTATTACGAACATGG...
ENST00000558445.6:c.135-16_135-15insATAGAACAATATCTATTACGAACATGGG ENSP00000452946.2:n.135-16_135-15insATAGAACAATATCTATTACGAACAT...
ENST00000559177.6:c.135-16_135-15insATAGAACAATATCTATTACGAACATGGG ENSP00000453477.2:n.135-16_135-15insATAGAACAATATCTATTACGAACAT...
ENST00000559179.2:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG ENSP00000453851.1:n.18-16_18-15insATAGAACAATATCTATTACGAACATGG...
ENST00000256552.11:c.84-16_84-15insATAGAACAATATCTATTACGAACATGGG MANE Select ENSP00000256552.7:n.84-16_84-15insATAGAACAATATCTATTACGAACATGG...
ENST00000256552.10:c.84-16_84-15insATAGAACAATATCTATTACGAACATGGG ENSP00000256552.6:n.84-16_84-15insATAGAACAATATCTATTACGAACATGG...
ENST00000397795.6:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG ENSP00000380897.2:n.18-16_18-15insATAGAACAATATCTATTACGAACATGG...
ENST00000542188.5:c.135-16_135-15insATAGAACAATATCTATTACGAACATGGG ENSP00000437849.1:n.135-16_135-15insATAGAACAATATCTATTACGAACAT...
ENST00000558445.5:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG ENSP00000452946.1:n.18-16_18-15insATAGAACAATATCTATTACGAACATGG...
ENST00000559177.5:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG ENSP00000453477.1:n.18-16_18-15insATAGAACAATATCTATTACGAACATGG...
ENST00000559179.1:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG ENSP00000453851.1:n.18-16_18-15insATAGAACAATATCTATTACGAACATGG...
ENST00000560658.5:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG ENSP00000454077.1:n.18-16_18-15insATAGAACAATATCTATTACGAACATGG...
NM_001252020.1:c.135-16_135-15insATAGAACAATATCTATTACGAACATGGG NP_001238949.1:n.135-16_135-15insATAGAACAATATCTATTACGAACATGGG...
NM_001252024.1:c.84-16_84-15insATAGAACAATATCTATTACGAACATGGG NP_001238953.1:n.84-16_84-15insATAGAACAATATCTATTACGAACATGGG
NM_001252030.1:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG NP_001238959.1:n.18-16_18-15insATAGAACAATATCTATTACGAACATGGG
NM_002420.5:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG NP_002411.3:n.18-16_18-15insATAGAACAATATCTATTACGAACATGGG
NM_001252024.2:c.84-16_84-15insATAGAACAATATCTATTACGAACATGGG MANE Select NP_001238953.1:n.84-16_84-15insATAGAACAATATCTATTACGAACATGGG
NM_001252030.2:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG NP_001238959.1:n.18-16_18-15insATAGAACAATATCTATTACGAACATGGG
NM_002420.6:c.18-16_18-15insATAGAACAATATCTATTACGAACATGGG NP_002411.3:n.18-16_18-15insATAGAACAATATCTATTACGAACATGGG
NM_001252020.2:c.135-16_135-15insATAGAACAATATCTATTACGAACATGGG NP_001238949.1:n.135-16_135-15insATAGAACAATATCTATTACGAACATGGG...