Canonical Allele Identifier: CA2013431479
Gene: KCNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045967C= , CM000674.2:g.5045967C= GRCh38
NC_000012.11:g.5155133C= , CM000674.1:g.5155133C= GRCh37
NC_000012.10:g.5025394C= NCBI36
NG_012198.1:g.7049C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252321.5:c.1820C= MANE Select ENSP00000252321.3:p.Thr607=
ENST00000252321.4:c.1820C= ENSP00000252321.3:p.Thr607=
NM_002234.3:c.1820C= NP_002225.2:p.Thr607=
NM_002234.4:c.1820C= MANE Select NP_002225.2:p.Thr607=