Canonical Allele Identifier: CA1330889669
Gene: KCNE4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223053178C= , CM000664.2:g.223053178C= GRCh38
NC_000002.11:g.223917896C= , CM000664.1:g.223917896C= GRCh37
NC_000002.10:g.223626140C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000281830.4:c.348C= MANE Select ENSP00000281830.5:p.Thr116=
ENST00000281830.3:c.501C= ENSP00000281830.4:p.Thr167=
ENST00000488477.2:n.75+904C=
NM_080671.3:c.501C= NP_542402.3:p.Thr167=
NM_080671.4:c.348C= MANE Select NP_542402.4:p.Thr116=