Canonical Allele Identifier: CA477703187

Gene: KCNJ1

Linked Data

• ClinVar Variation Id: 2864371
• ClinVar RCV Id: RCV003702701
• MyVariant Identifiers: chr11:g.128709914G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128840019G>A , CM000673.2:g.128840019G>A	GRCh38
NC_000011.9:g.128709914G>A , CM000673.1:g.128709914G>A	GRCh37
NC_000011.8:g.128215124G>A	NCBI36
NG_009379.1:g.32355C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.225C>T MANE Select	ENSP00000376434.1:p.Phe75=
ENST00000324003.3:c.225C>T	ENSP00000316136.3:p.Phe75=
ENST00000324036.7:c.225C>T	ENSP00000316233.3:p.Phe75=
ENST00000392664.2:c.282C>T	ENSP00000376432.2:p.Phe94=
ENST00000392665.6:c.225C>T	ENSP00000376433.2:p.Phe75=
ENST00000392666.5:c.225C>T	ENSP00000376434.1:p.Phe75=
ENST00000440599.6:c.225C>T	ENSP00000406320.2:p.Phe75=
NM_000220.4:c.282C>T	NP_000211.1:p.Phe94=
NM_153764.2:c.225C>T	NP_722448.1:p.Phe75=
NM_153765.2:c.276C>T	NP_722449.3:p.Phe92=
NM_153766.2:c.225C>T	NP_722450.1:p.Phe75=
NM_153767.3:c.225C>T	NP_722451.1:p.Phe75=
NM_000220.6:c.282C>T	NP_000211.1:p.Phe94=
NM_153764.3:c.225C>T	NP_722448.1:p.Phe75=
NM_153765.3:c.276C>T	NP_722449.3:p.Phe92=
NM_153766.3:c.225C>T MANE Select	NP_722450.1:p.Phe75=
NM_153767.4:c.225C>T	NP_722451.1:p.Phe75=