Canonical Allele Identifier: CA351121573
Gene: KCNE4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.223917996A>C (hg19) chr2:g.223053278A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.223053278A>C , CM000664.2:g.223053278A>C GRCh38
NC_000002.11:g.223917996A>C , CM000664.1:g.223917996A>C GRCh37
NC_000002.10:g.223626240A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000281830.4:c.448A>C MANE Select ENSP00000281830.5:p.Thr150Pro
ENST00000281830.3:c.601A>C ENSP00000281830.4:p.Thr201Pro
ENST00000488477.2:n.75+1004A>C
NM_080671.3:c.601A>C NP_542402.3:p.Thr201Pro
NM_080671.4:c.448A>C MANE Select NP_542402.4:p.Thr150Pro
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