Canonical Allele Identifier: CA320436764

Gene: KCNE1

Linked Data

• dbSNP Id: rs73207020
• gnomAD v2: 21-35880007-T-C
• gnomAD v3: 21-34507709-T-C
• gnomAD v4: 21-34507709-T-C
• MyVariant Identifiers: chr21:g.35880007T>C (hg19) ; chr21:g.34507709T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.34507709T>C , CM000683.2:g.34507709T>C	GRCh38
NC_000021.8:g.35880007T>C , CM000683.1:g.35880007T>C	GRCh37
NC_000021.7:g.34801877T>C	NCBI36
NG_009091.1:g.8607A>G , LRG_290:g.8607A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000683028.1:n.403-1951A>G
ENST00000683564.1:n.403+3392A>G
ENST00000684073.1:n.404-1951A>G
ENST00000684327.1:n.403+3392A>G
ENST00000684616.1:n.465-1951A>G
ENST00000399286.3:c.-162+3392A>G MANE Select	ENSP00000382226.2:n.-162+3392A>G
ENST00000337385.7:c.-162+3392A>G	ENSP00000337255.3:n.-162+3392A>G
ENST00000399284.1:c.-134+3392A>G	ENSP00000382225.1:n.-134+3392A>G
ENST00000399286.2:c.-162+3392A>G	ENSP00000382226.2:n.-162+3392A>G
ENST00000611936.1:c.-51+3392A>G	ENSP00000478215.1:n.-51+3392A>G
NM_000219.5:c.-162+3392A>G	NP_000210.2:n.-162+3392A>G
NM_001270402.2:c.-162+3392A>G	NP_001257331.1:n.-162+3392A>G
NM_001270403.2:c.-134+3392A>G	NP_001257332.1:n.-134+3392A>G
NM_001270404.2:c.-51+3392A>G	NP_001257333.1:n.-51+3392A>G
XM_011529557.1:c.168+3392A>G	XP_011527859.1:n.168+3392A>G
NM_000219.6:c.-162+3392A>G MANE Select	NP_000210.2:n.-162+3392A>G
NM_001270402.3:c.-162+3392A>G	NP_001257331.1:n.-162+3392A>G
NM_001270404.3:c.-51+3392A>G	NP_001257333.1:n.-51+3392A>G