Canonical Allele Identifier: CA5902163

Gene: KCNJ11

Linked Data

• dbSNP Id: rs759913615
• ExAC: 11:17408444 G / T
• gnomAD v2: 11-17408444-G-T
• gnomAD v3: 11-17386897-G-T
• gnomAD v4: 11-17386897-G-T
• MyVariant Identifiers: chr11:g.17408444G>T (hg19) ; chr11:g.17386897G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386897G>T , CM000673.2:g.17386897G>T	GRCh38
NC_000011.9:g.17408444G>T , CM000673.1:g.17408444G>T	GRCh37
NC_000011.8:g.17365020G>T	NCBI36
NG_012446.1:g.6763C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682350.1:c.*22C>A	ENSP00000508090.1:n.*22C>A
ENST00000682764.1:c.*22C>A	ENSP00000506780.1:n.*22C>A
ENST00000339994.5:c.*22C>A MANE Select	ENSP00000345708.4:n.*22C>A
ENST00000339994.4:c.*22C>A	ENSP00000345708.4:n.*22C>A
ENST00000528731.1:c.*22C>A	ENSP00000434755.1:n.*22C>A
NM_000525.3:c.*22C>A	NP_000516.3:n.*22C>A
NM_001166290.1:c.*22C>A	NP_001159762.1:n.*22C>A
XM_006718226.2:c.*22C>A	XP_006718289.1:n.*22C>A
XR_930867.1:n.1353C>A
XM_006718226.3:c.*22C>A	XP_006718289.1:n.*22C>A
XM_017017680.1:c.*22C>A	XP_016873169.1:n.*22C>A
NM_001166290.2:c.*22C>A	NP_001159762.1:n.*22C>A
NM_001377296.1:c.*22C>A	NP_001364225.1:n.*22C>A
NM_001377297.1:c.*22C>A	NP_001364226.1:n.*22C>A
NM_000525.4:c.*22C>A MANE Select	NP_000516.3:n.*22C>A