Canonical Allele Identifier: CA478096027
Gene: KCNA5 HGNC NCBI

Linked Data

gnomAD v4: 12-5045626-C-A
MyVariant Identifiers: chr12:g.5154792C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045626C>A , CM000674.2:g.5045626C>A GRCh38
NC_000012.11:g.5154792C>A , CM000674.1:g.5154792C>A GRCh37
NC_000012.10:g.5025053C>A NCBI36
NG_012198.1:g.6708C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1479C>A MANE Select ENSP00000252321.3:p.Gly493=
ENST00000252321.4:c.1479C>A ENSP00000252321.3:p.Gly493=
NM_002234.3:c.1479C>A NP_002225.2:p.Gly493=
NM_002234.4:c.1479C>A MANE Select NP_002225.2:p.Gly493=
Search 100 bp 5'
Search 100 bp 3'