Canonical Allele Identifier: CA383247109

Gene: KCNJ1

Linked Data

• gnomAD v4: 11-128840098-A-G
• MyVariant Identifiers: chr11:g.128709993A>G (hg19) ; chr11:g.128840098A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128840098A>G , CM000673.2:g.128840098A>G	GRCh38
NC_000011.9:g.128709993A>G , CM000673.1:g.128709993A>G	GRCh37
NC_000011.8:g.128215203A>G	NCBI36
NG_009379.1:g.32276T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.146T>C MANE Select	ENSP00000376434.1:p.Ile49Thr
ENST00000324003.3:c.146T>C	ENSP00000316136.3:p.Ile49Thr
ENST00000324036.7:c.146T>C	ENSP00000316233.3:p.Ile49Thr
ENST00000392664.2:c.203T>C	ENSP00000376432.2:p.Ile68Thr
ENST00000392665.6:c.146T>C	ENSP00000376433.2:p.Ile49Thr
ENST00000392666.5:c.146T>C	ENSP00000376434.1:p.Ile49Thr
ENST00000440599.6:c.146T>C	ENSP00000406320.2:p.Ile49Thr
ENST00000531562.1:n.491T>C
NM_000220.4:c.203T>C	NP_000211.1:p.Ile68Thr
NM_153764.2:c.146T>C	NP_722448.1:p.Ile49Thr
NM_153765.2:c.197T>C	NP_722449.3:p.Ile66Thr
NM_153766.2:c.146T>C	NP_722450.1:p.Ile49Thr
NM_153767.3:c.146T>C	NP_722451.1:p.Ile49Thr
NM_000220.6:c.203T>C	NP_000211.1:p.Ile68Thr
NM_153764.3:c.146T>C	NP_722448.1:p.Ile49Thr
NM_153765.3:c.197T>C	NP_722449.3:p.Ile66Thr
NM_153766.3:c.146T>C MANE Select	NP_722450.1:p.Ile49Thr
NM_153767.4:c.146T>C	NP_722451.1:p.Ile49Thr