Canonical Allele Identifier: CA1933118089
Gene: CALHM1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.103454023A= , CM000672.2:g.103454023A= GRCh38
NC_000010.10:g.105213780A= , CM000672.1:g.105213780A= GRCh37
NC_000010.9:g.105203770A= NCBI36
NG_016855.1:g.9869T=

Transcript Alleles

HGVS Amino-acid change
ENST00000329905.6:c.*1239T= MANE Select ENSP00000329926.6:n.*1239T=
ENST00000329905.5:c.*1239T= ENSP00000329926.5:n.*1239T=
NM_001001412.3:c.*1239T= NP_001001412.3:n.*1239T=
NM_001001412.4:c.*1239T= MANE Select NP_001001412.3:n.*1239T=
Search 100 bp 5'
Search 100 bp 3'