Canonical Allele Identifier: CA2008278864

Gene: KCNJ1

Linked Data

• dbSNP Id: rs2855800

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128861060A>T , CM000673.2:g.128861060A>T	GRCh38
NC_000011.9:g.128730955A>T , CM000673.1:g.128730955A>T	GRCh37
NC_000011.8:g.128236165A>T	NCBI36
NG_009379.1:g.11314T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000392666.6:c.-192+6113T>A MANE Select	ENSP00000376434.1:n.-192+6113T>A
ENST00000324003.3:c.-192+6113T>A	ENSP00000316136.3:n.-192+6113T>A
ENST00000324036.7:c.-192+5463T>A	ENSP00000316233.3:n.-192+5463T>A
ENST00000392665.6:c.-22+6113T>A	ENSP00000376433.2:n.-22+6113T>A
ENST00000392666.5:c.-192+6113T>A	ENSP00000376434.1:n.-192+6113T>A
ENST00000440599.6:c.-22+5463T>A	ENSP00000406320.2:n.-22+5463T>A
ENST00000531562.1:n.124+6113T>A
NM_153764.2:c.-22+6113T>A	NP_722448.1:n.-22+6113T>A
NM_153765.2:c.30+5463T>A	NP_722449.3:n.30+5463T>A
NM_153766.2:c.-192+6113T>A	NP_722450.1:n.-192+6113T>A
NM_153767.3:c.-192+5463T>A	NP_722451.1:n.-192+5463T>A
XR_001748442.1:n.3419-2837A>T
NM_153764.3:c.-22+6113T>A	NP_722448.1:n.-22+6113T>A
NM_153765.3:c.30+5463T>A	NP_722449.3:n.30+5463T>A
NM_153766.3:c.-192+6113T>A MANE Select	NP_722450.1:n.-192+6113T>A
NM_153767.4:c.-192+5463T>A	NP_722451.1:n.-192+5463T>A