Canonical Allele Identifier: CA1933118094
Gene: CALHM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103454026T= , CM000672.2:g.103454026T= GRCh38
NC_000010.10:g.105213783T= , CM000672.1:g.105213783T= GRCh37
NC_000010.9:g.105203773T= NCBI36
NG_016855.1:g.9866A=

Transcript Alleles

HGVS Amino-acid change
ENST00000329905.6:c.*1236A= MANE Select ENSP00000329926.6:n.*1236A=
ENST00000329905.5:c.*1236A= ENSP00000329926.5:n.*1236A=
NM_001001412.3:c.*1236A= NP_001001412.3:n.*1236A=
NM_001001412.4:c.*1236A= MANE Select NP_001001412.3:n.*1236A=