Canonical Allele Identifier: CA478096054
Gene: KCNA5 HGNC NCBI

Linked Data

gnomAD v4: 12-5045988-G-A
MyVariant Identifiers: chr12:g.5155154G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045988G>A , CM000674.2:g.5045988G>A GRCh38
NC_000012.11:g.5155154G>A , CM000674.1:g.5155154G>A GRCh37
NC_000012.10:g.5025415G>A NCBI36
NG_012198.1:g.7070G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252321.5:c.1841G>A MANE Select ENSP00000252321.3:p.Ter614=
ENST00000252321.4:c.1841G>A ENSP00000252321.3:p.Ter614=
NM_002234.3:c.1841G>A NP_002225.2:p.Ter614=
NM_002234.4:c.1841G>A MANE Select NP_002225.2:p.Ter614=