Canonical Allele Identifier: CA431669532
Gene: KCNE4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.223917890C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223053172C>A , CM000664.2:g.223053172C>A GRCh38
NC_000002.11:g.223917890C>A , CM000664.1:g.223917890C>A GRCh37
NC_000002.10:g.223626134C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000281830.4:c.342C>A MANE Select ENSP00000281830.5:p.Ser114=
ENST00000281830.3:c.495C>A ENSP00000281830.4:p.Ser165=
ENST00000488477.2:n.75+898C>A
NM_080671.3:c.495C>A NP_542402.3:p.Ser165=
NM_080671.4:c.342C>A MANE Select NP_542402.4:p.Ser114=