Canonical Allele Identifier: CA478095900
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs1304613766
gnomAD v2: 12-5154735-A-G
gnomAD v4: 12-5045569-A-G
MyVariant Identifiers: chr12:g.5154735A>G (hg19) chr12:g.5045569A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045569A>G , CM000674.2:g.5045569A>G GRCh38
NC_000012.11:g.5154735A>G , CM000674.1:g.5154735A>G GRCh37
NC_000012.10:g.5024996A>G NCBI36
NG_012198.1:g.6651A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1422A>G MANE Select ENSP00000252321.3:p.Ala474=
ENST00000252321.4:c.1422A>G ENSP00000252321.3:p.Ala474=
NM_002234.3:c.1422A>G NP_002225.2:p.Ala474=
NM_002234.4:c.1422A>G MANE Select NP_002225.2:p.Ala474=
Search 100 bp 5'
Search 100 bp 3'