Canonical Allele Identifier: CA1933125302
Gene: CALHM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458411C= , CM000672.2:g.103458411C= GRCh38
NC_000010.10:g.105218168C= , CM000672.1:g.105218168C= GRCh37
NC_000010.9:g.105208158C= NCBI36
NG_016855.1:g.5481G=

Transcript Alleles

HGVS Amino-acid change
ENST00000329905.6:c.341G= MANE Select ENSP00000329926.6:p.Trp114=
ENST00000329905.5:c.341G= ENSP00000329926.5:p.Trp114=
NM_001001412.3:c.341G= NP_001001412.3:p.Trp114=
NM_001001412.4:c.341G= MANE Select NP_001001412.3:p.Trp114=