Canonical Allele Identifier: CA383465213
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs1350480561
gnomAD v2: 12-5154128-T-A
gnomAD v4: 12-5044962-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044962T>A , CM000674.2:g.5044962T>A GRCh38
NC_000012.11:g.5154128T>A , CM000674.1:g.5154128T>A GRCh37
NC_000012.10:g.5024389T>A NCBI36
NG_012198.1:g.6044T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.815T>A MANE Select ENSP00000252321.3:p.Leu272Gln
ENST00000252321.4:c.815T>A ENSP00000252321.3:p.Leu272Gln
NM_002234.3:c.815T>A NP_002225.2:p.Leu272Gln
NM_002234.4:c.815T>A MANE Select NP_002225.2:p.Leu272Gln