Canonical Allele Identifier: CA1933124990
Gene: CALHM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103458305G= , CM000672.2:g.103458305G= GRCh38
NC_000010.10:g.105218062G= , CM000672.1:g.105218062G= GRCh37
NC_000010.9:g.105208052G= NCBI36
NG_016855.1:g.5587C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000329905.6:c.447C= MANE Select ENSP00000329926.6:p.Ala149=
ENST00000329905.5:c.447C= ENSP00000329926.5:p.Ala149=
NM_001001412.3:c.447C= NP_001001412.3:p.Ala149=
NM_001001412.4:c.447C= MANE Select NP_001001412.3:p.Ala149=