Canonical Allele Identifier: CA383466137
Gene: KCNA5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045423A>T , CM000674.2:g.5045423A>T GRCh38
NC_000012.11:g.5154589A>T , CM000674.1:g.5154589A>T GRCh37
NC_000012.10:g.5024850A>T NCBI36
NG_012198.1:g.6505A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1276A>T MANE Select ENSP00000252321.3:p.Thr426Ser
ENST00000252321.4:c.1276A>T ENSP00000252321.3:p.Thr426Ser
NM_002234.3:c.1276A>T NP_002225.2:p.Thr426Ser
NM_002234.4:c.1276A>T MANE Select NP_002225.2:p.Thr426Ser