Canonical Allele Identifier: CA351121329
Gene: KCNE4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.223917886T>C (hg19) chr2:g.223053168T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223053168T>C , CM000664.2:g.223053168T>C GRCh38
NC_000002.11:g.223917886T>C , CM000664.1:g.223917886T>C GRCh37
NC_000002.10:g.223626130T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000281830.4:c.338T>C MANE Select ENSP00000281830.5:p.Leu113Pro
ENST00000281830.3:c.491T>C ENSP00000281830.4:p.Leu164Pro
ENST00000488477.2:n.75+894T>C
NM_080671.3:c.491T>C NP_542402.3:p.Leu164Pro
NM_080671.4:c.338T>C MANE Select NP_542402.4:p.Leu113Pro
Search 100 bp 5'
Search 100 bp 3'