Canonical Allele Identifier: CA478094427
Gene: KCNA5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5153319G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044153G>A , CM000674.2:g.5044153G>A GRCh38
NC_000012.11:g.5153319G>A , CM000674.1:g.5153319G>A GRCh37
NC_000012.10:g.5023580G>A NCBI36
NG_012198.1:g.5235G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252321.5:c.6G>A MANE Select ENSP00000252321.3:p.Glu2=
ENST00000252321.4:c.6G>A ENSP00000252321.3:p.Glu2=
NM_002234.3:c.6G>A NP_002225.2:p.Glu2=
NM_002234.4:c.6G>A MANE Select NP_002225.2:p.Glu2=
Search 100 bp 5'
Search 100 bp 3'