Canonical Allele Identifier: CA2013431478
Gene: KCNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045966A= , CM000674.2:g.5045966A= GRCh38
NC_000012.11:g.5155132A= , CM000674.1:g.5155132A= GRCh37
NC_000012.10:g.5025393A= NCBI36
NG_012198.1:g.7048A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1819A= MANE Select ENSP00000252321.3:p.Thr607=
ENST00000252321.4:c.1819A= ENSP00000252321.3:p.Thr607=
NM_002234.3:c.1819A= NP_002225.2:p.Thr607=
NM_002234.4:c.1819A= MANE Select NP_002225.2:p.Thr607=