Canonical Allele Identifier: CA477703311

Gene: KCNJ1

Linked Data

• MyVariant Identifiers: chr11:g.128709593G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839698G>A , CM000673.2:g.128839698G>A	GRCh38
NC_000011.9:g.128709593G>A , CM000673.1:g.128709593G>A	GRCh37
NC_000011.8:g.128214803G>A	NCBI36
NG_009379.1:g.32676C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.546C>T MANE Select	ENSP00000376434.1:p.Ser182=
ENST00000324036.7:c.546C>T	ENSP00000316233.3:p.Ser182=
ENST00000392664.2:c.603C>T	ENSP00000376432.2:p.Ser201=
ENST00000392665.6:c.546C>T	ENSP00000376433.2:p.Ser182=
ENST00000392666.5:c.546C>T	ENSP00000376434.1:p.Ser182=
ENST00000440599.6:c.546C>T	ENSP00000406320.2:p.Ser182=
NM_000220.4:c.603C>T	NP_000211.1:p.Ser201=
NM_153764.2:c.546C>T	NP_722448.1:p.Ser182=
NM_153765.2:c.597C>T	NP_722449.3:p.Ser199=
NM_153766.2:c.546C>T	NP_722450.1:p.Ser182=
NM_153767.3:c.546C>T	NP_722451.1:p.Ser182=
NM_000220.6:c.603C>T	NP_000211.1:p.Ser201=
NM_153764.3:c.546C>T	NP_722448.1:p.Ser182=
NM_153765.3:c.597C>T	NP_722449.3:p.Ser199=
NM_153766.3:c.546C>T MANE Select	NP_722450.1:p.Ser182=
NM_153767.4:c.546C>T	NP_722451.1:p.Ser182=