Canonical Allele Identifier: CA6357416

Gene: KCNJ1

Linked Data

• ClinVar Variation Id: 303569
• ClinVar RCV Id: RCV000344532
• dbSNP Id: rs746292586
• ExAC: 11:128709216 G / A
• gnomAD v2: 11-128709216-G-A
• gnomAD v4: 11-128839321-G-A
• MyVariant Identifiers: chr11:g.128709216G>A (hg19) ; chr11:g.128839321G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839321G>A , CM000673.2:g.128839321G>A	GRCh38
NC_000011.9:g.128709216G>A , CM000673.1:g.128709216G>A	GRCh37
NC_000011.8:g.128214426G>A	NCBI36
NG_009379.1:g.33053C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.923C>T MANE Select	ENSP00000376434.1:p.Pro308Leu
ENST00000324036.7:c.923C>T	ENSP00000316233.3:p.Pro308Leu
ENST00000392664.2:c.980C>T	ENSP00000376432.2:p.Pro327Leu
ENST00000392665.6:c.923C>T	ENSP00000376433.2:p.Pro308Leu
ENST00000392666.5:c.923C>T	ENSP00000376434.1:p.Pro308Leu
ENST00000440599.6:c.923C>T	ENSP00000406320.2:p.Pro308Leu
NM_000220.4:c.980C>T	NP_000211.1:p.Pro327Leu
NM_153764.2:c.923C>T	NP_722448.1:p.Pro308Leu
NM_153765.2:c.974C>T	NP_722449.3:p.Pro325Leu
NM_153766.2:c.923C>T	NP_722450.1:p.Pro308Leu
NM_153767.3:c.923C>T	NP_722451.1:p.Pro308Leu
NM_000220.6:c.980C>T	NP_000211.1:p.Pro327Leu
NM_153764.3:c.923C>T	NP_722448.1:p.Pro308Leu
NM_153765.3:c.974C>T	NP_722449.3:p.Pro325Leu
NM_153766.3:c.923C>T MANE Select	NP_722450.1:p.Pro308Leu
NM_153767.4:c.923C>T	NP_722451.1:p.Pro308Leu