Canonical Allele Identifier: CA1330889657
Gene: KCNE4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223053155G= , CM000664.2:g.223053155G= GRCh38
NC_000002.11:g.223917873G= , CM000664.1:g.223917873G= GRCh37
NC_000002.10:g.223626117G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000281830.4:c.325G= MANE Select ENSP00000281830.5:p.Val109=
ENST00000281830.3:c.478G= ENSP00000281830.4:p.Val160=
ENST00000488477.2:n.75+881G=
NM_080671.3:c.478G= NP_542402.3:p.Val160=
NM_080671.4:c.325G= MANE Select NP_542402.4:p.Val109=