Canonical Allele Identifier: CA379775066

Gene: KCNJ11

Linked Data

• dbSNP Id: rs1213486296
• gnomAD v2: 11-17409385-A-T
• gnomAD v4: 11-17387838-A-T
• MyVariant Identifiers: chr11:g.17409385A>T (hg19) ; chr11:g.17387838A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387838A>T , CM000673.2:g.17387838A>T	GRCh38
NC_000011.9:g.17409385A>T , CM000673.1:g.17409385A>T	GRCh37
NC_000011.8:g.17365961A>T	NCBI36
NG_012446.1:g.5822T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000528992.2:c.26T>A	ENSP00000436479.2:p.Leu9His
ENST00000682350.1:c.-8T>A	ENSP00000508090.1:n.-8T>A
ENST00000682764.1:c.-8T>A	ENSP00000506780.1:n.-8T>A
ENST00000339994.5:c.254T>A MANE Select	ENSP00000345708.4:p.Leu85His
ENST00000339994.4:c.254T>A	ENSP00000345708.4:p.Leu85His
ENST00000526912.1:c.-8T>A	ENSP00000432729.1:n.-8T>A
ENST00000528731.1:c.-8T>A	ENSP00000434755.1:n.-8T>A
ENST00000528992.1:c.271T>A
NM_000525.3:c.254T>A	NP_000516.3:p.Leu85His
NM_001166290.1:c.-8T>A	NP_001159762.1:n.-8T>A
XM_006718226.2:c.-8T>A	XP_006718289.1:n.-8T>A
XR_930867.1:n.412T>A
XM_006718226.3:c.-8T>A	XP_006718289.1:n.-8T>A
XM_017017680.1:c.-8T>A	XP_016873169.1:n.-8T>A
NM_001166290.2:c.-8T>A	NP_001159762.1:n.-8T>A
NM_001377296.1:c.-8T>A	NP_001364225.1:n.-8T>A
NM_001377297.1:c.-8T>A	NP_001364226.1:n.-8T>A
NM_000525.4:c.254T>A MANE Select	NP_000516.3:p.Leu85His