Canonical Allele Identifier: CA477703065

Gene: KCNJ1

Linked Data

• ClinVar Variation Id: 2787050
• ClinVar RCV Id: RCV003660533
• dbSNP Id: rs1301070689
• gnomAD v2: 11-128709836-G-A
• gnomAD v3: 11-128839941-G-A
• gnomAD v4: 11-128839941-G-A
• MyVariant Identifiers: chr11:g.128709836G>A (hg19) ; chr11:g.128839941G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839941G>A , CM000673.2:g.128839941G>A	GRCh38
NC_000011.9:g.128709836G>A , CM000673.1:g.128709836G>A	GRCh37
NC_000011.8:g.128215046G>A	NCBI36
NG_009379.1:g.32433C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.303C>T MANE Select	ENSP00000376434.1:p.Pro101=
ENST00000324003.3:c.303C>T	ENSP00000316136.3:p.Pro101=
ENST00000324036.7:c.303C>T	ENSP00000316233.3:p.Pro101=
ENST00000392664.2:c.360C>T	ENSP00000376432.2:p.Pro120=
ENST00000392665.6:c.303C>T	ENSP00000376433.2:p.Pro101=
ENST00000392666.5:c.303C>T	ENSP00000376434.1:p.Pro101=
ENST00000440599.6:c.303C>T	ENSP00000406320.2:p.Pro101=
NM_000220.4:c.360C>T	NP_000211.1:p.Pro120=
NM_153764.2:c.303C>T	NP_722448.1:p.Pro101=
NM_153765.2:c.354C>T	NP_722449.3:p.Pro118=
NM_153766.2:c.303C>T	NP_722450.1:p.Pro101=
NM_153767.3:c.303C>T	NP_722451.1:p.Pro101=
NM_000220.6:c.360C>T	NP_000211.1:p.Pro120=
NM_153764.3:c.303C>T	NP_722448.1:p.Pro101=
NM_153765.3:c.354C>T	NP_722449.3:p.Pro118=
NM_153766.3:c.303C>T MANE Select	NP_722450.1:p.Pro101=
NM_153767.4:c.303C>T	NP_722451.1:p.Pro101=