Canonical Allele Identifier: CA6357937

Gene: KCNJ5

Linked Data

• ClinVar Variation Id: 3232296
• ClinVar RCV Id: RCV004520979
• dbSNP Id: rs753852908
• ExAC: 11:128781956 C / T
• gnomAD v2: 11-128781956-C-T
• gnomAD v3: 11-128912061-C-T
• gnomAD v4: 11-128912061-C-T
• COSMIC: COSM4694435
• MyVariant Identifiers: chr11:g.128781956C>T (hg19) ; chr11:g.128912061C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128912061C>T , CM000673.2:g.128912061C>T	GRCh38
NC_000011.9:g.128781956C>T , CM000673.1:g.128781956C>T	GRCh37
NC_000011.8:g.128287166C>T	NCBI36
NG_023406.2:g.25644C>T , LRG_333:g.25644C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529694.6:c.788C>T MANE Select	ENSP00000433295.1:p.Thr263Met
ENST00000338350.4:c.788C>T	ENSP00000339960.4:p.Thr263Met
ENST00000529694.5:c.788C>T	ENSP00000433295.1:p.Thr263Met
ENST00000533599.1:c.788C>T	ENSP00000434266.1:p.Thr263Met
NM_000890.3:c.788C>T , LRG_333t1:c.788C>T	NP_000881.3:p.Thr263Met
XM_011542809.1:c.788C>T	XP_011541111.1:p.Thr263Met
XM_011542810.1:c.788C>T	XP_011541112.1:p.Thr263Met
NM_000890.4:c.788C>T	NP_000881.3:p.Thr263Met
NM_001354169.1:c.788C>T	NP_001341098.1:p.Thr263Met
XM_011542809.2:c.788C>T	XP_011541111.1:p.Thr263Met
XM_011542810.3:c.788C>T	XP_011541112.1:p.Thr263Met
NM_000890.5:c.788C>T MANE Select	NP_000881.3:p.Thr263Met
NM_001354169.2:c.788C>T	NP_001341098.1:p.Thr263Met