Canonical Allele Identifier: CA1933118091
Gene: CALHM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103454025C= , CM000672.2:g.103454025C= GRCh38
NC_000010.10:g.105213782C= , CM000672.1:g.105213782C= GRCh37
NC_000010.9:g.105203772C= NCBI36
NG_016855.1:g.9867G=

Transcript Alleles

HGVS Amino-acid change
ENST00000329905.6:c.*1237G= MANE Select ENSP00000329926.6:n.*1237G=
ENST00000329905.5:c.*1237G= ENSP00000329926.5:n.*1237G=
NM_001001412.3:c.*1237G= NP_001001412.3:n.*1237G=
NM_001001412.4:c.*1237G= MANE Select NP_001001412.3:n.*1237G=