Canonical Allele Identifier: CA477704190

Gene: KCNJ5

Linked Data

• ClinVar Variation Id: 1103043
• ClinVar RCV Id: RCV001426595
• dbSNP Id: rs2136004112
• MyVariant Identifiers: chr11:g.128786527G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128916632G>C , CM000673.2:g.128916632G>C	GRCh38
NC_000011.9:g.128786527G>C , CM000673.1:g.128786527G>C	GRCh37
NC_000011.8:g.128291737G>C	NCBI36
NG_023406.2:g.30215G>C , LRG_333:g.30215G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000529694.6:c.1161G>C MANE Select	ENSP00000433295.1:p.Gly387=
ENST00000338350.4:c.1161G>C	ENSP00000339960.4:p.Gly387=
ENST00000529694.5:c.1161G>C	ENSP00000433295.1:p.Gly387=
ENST00000533599.1:c.1161G>C	ENSP00000434266.1:p.Gly387=
NM_000890.3:c.1161G>C , LRG_333t1:c.1161G>C	NP_000881.3:p.Gly387=
XM_011542809.1:c.1161G>C	XP_011541111.1:p.Gly387=
XM_011542810.1:c.1161G>C	XP_011541112.1:p.Gly387=
NM_000890.4:c.1161G>C	NP_000881.3:p.Gly387=
NM_001354169.1:c.1161G>C	NP_001341098.1:p.Gly387=
XM_011542809.2:c.1161G>C	XP_011541111.1:p.Gly387=
XM_011542810.3:c.1161G>C	XP_011541112.1:p.Gly387=
NM_000890.5:c.1161G>C MANE Select	NP_000881.3:p.Gly387=
NM_001354169.2:c.1161G>C	NP_001341098.1:p.Gly387=