Canonical Allele Identifier: CA2342626695
Gene: CACNG8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.53977809T= , CM000681.2:g.53977809T= GRCh38
NC_000019.9:g.54481063T= , CM000681.1:g.54481063T= GRCh37
NC_000019.8:g.59172875T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000270458.4:c.284-337T= MANE Select ENSP00000270458.3:n.284-337T=
ENST00000270458.2:c.284-337T= ENSP00000270458.2:n.284-337T=
NM_031895.5:c.284-337T= NP_114101.4:n.284-337T=
NM_031895.6:c.284-337T= MANE Select NP_114101.4:n.284-337T=