Canonical Allele Identifier: CA6357436

Gene: KCNJ1

Linked Data

• ClinVar Variation Id: 586076
• ClinVar RCV Id: RCV000712086 ; RCV001784350
• dbSNP Id: rs746509804
• ExAC: 11:128709272 G / T
• gnomAD v2: 11-128709272-G-T
• gnomAD v3: 11-128839377-G-T
• gnomAD v4: 11-128839377-G-T
• MyVariant Identifiers: chr11:g.128709272G>T (hg19) ; chr11:g.128839377G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839377G>T , CM000673.2:g.128839377G>T	GRCh38
NC_000011.9:g.128709272G>T , CM000673.1:g.128709272G>T	GRCh37
NC_000011.8:g.128214482G>T	NCBI36
NG_009379.1:g.32997C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.867C>A MANE Select	ENSP00000376434.1:p.Cys289Ter
ENST00000324036.7:c.867C>A	ENSP00000316233.3:p.Cys289Ter
ENST00000392664.2:c.924C>A	ENSP00000376432.2:p.Cys308Ter
ENST00000392665.6:c.867C>A	ENSP00000376433.2:p.Cys289Ter
ENST00000392666.5:c.867C>A	ENSP00000376434.1:p.Cys289Ter
ENST00000440599.6:c.867C>A	ENSP00000406320.2:p.Cys289Ter
NM_000220.4:c.924C>A	NP_000211.1:p.Cys308Ter
NM_153764.2:c.867C>A	NP_722448.1:p.Cys289Ter
NM_153765.2:c.918C>A	NP_722449.3:p.Cys306Ter
NM_153766.2:c.867C>A	NP_722450.1:p.Cys289Ter
NM_153767.3:c.867C>A	NP_722451.1:p.Cys289Ter
NM_000220.6:c.924C>A	NP_000211.1:p.Cys308Ter
NM_153764.3:c.867C>A	NP_722448.1:p.Cys289Ter
NM_153765.3:c.918C>A	NP_722449.3:p.Cys306Ter
NM_153766.3:c.867C>A MANE Select	NP_722450.1:p.Cys289Ter
NM_153767.4:c.867C>A	NP_722451.1:p.Cys289Ter