Canonical Allele Identifier: CA477702996

Gene: KCNJ1

Linked Data

• MyVariant Identifiers: chr11:g.128709401T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128839506T>A , CM000673.2:g.128839506T>A	GRCh38
NC_000011.9:g.128709401T>A , CM000673.1:g.128709401T>A	GRCh37
NC_000011.8:g.128214611T>A	NCBI36
NG_009379.1:g.32868A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392666.6:c.738A>T MANE Select	ENSP00000376434.1:p.Pro246=
ENST00000324036.7:c.738A>T	ENSP00000316233.3:p.Pro246=
ENST00000392664.2:c.795A>T	ENSP00000376432.2:p.Pro265=
ENST00000392665.6:c.738A>T	ENSP00000376433.2:p.Pro246=
ENST00000392666.5:c.738A>T	ENSP00000376434.1:p.Pro246=
ENST00000440599.6:c.738A>T	ENSP00000406320.2:p.Pro246=
NM_000220.4:c.795A>T	NP_000211.1:p.Pro265=
NM_153764.2:c.738A>T	NP_722448.1:p.Pro246=
NM_153765.2:c.789A>T	NP_722449.3:p.Pro263=
NM_153766.2:c.738A>T	NP_722450.1:p.Pro246=
NM_153767.3:c.738A>T	NP_722451.1:p.Pro246=
NM_000220.6:c.795A>T	NP_000211.1:p.Pro265=
NM_153764.3:c.738A>T	NP_722448.1:p.Pro246=
NM_153765.3:c.789A>T	NP_722449.3:p.Pro263=
NM_153766.3:c.738A>T MANE Select	NP_722450.1:p.Pro246=
NM_153767.4:c.738A>T	NP_722451.1:p.Pro246=