Canonical Allele Identifier: CA383466582
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs1862768169
gnomAD v3: 12-5045627-A-T
gnomAD v4: 12-5045627-A-T
MyVariant Identifiers: chr12:g.5154793A>T (hg19) chr12:g.5045627A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045627A>T , CM000674.2:g.5045627A>T GRCh38
NC_000012.11:g.5154793A>T , CM000674.1:g.5154793A>T GRCh37
NC_000012.10:g.5025054A>T NCBI36
NG_012198.1:g.6709A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1480A>T MANE Select ENSP00000252321.3:p.Lys494Ter
ENST00000252321.4:c.1480A>T ENSP00000252321.3:p.Lys494Ter
NM_002234.3:c.1480A>T NP_002225.2:p.Lys494Ter
NM_002234.4:c.1480A>T MANE Select NP_002225.2:p.Lys494Ter
Search 100 bp 5'
Search 100 bp 3'