Canonical Allele Identifier: CA5902344

Gene: KCNJ11

Linked Data

• dbSNP Id: rs746264957
• ExAC: 11:17409594 T / A
• gnomAD v2: 11-17409594-T-A
• gnomAD v4: 11-17388047-T-A
• MyVariant Identifiers: chr11:g.17409594T>A (hg19) ; chr11:g.17388047T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17388047T>A , CM000673.2:g.17388047T>A	GRCh38
NC_000011.9:g.17409594T>A , CM000673.1:g.17409594T>A	GRCh37
NC_000011.8:g.17366170T>A	NCBI36
NG_012446.1:g.5613A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000528992.2:c.-184A>T	ENSP00000436479.2:n.-184A>T
ENST00000682350.1:c.-16-201A>T	ENSP00000508090.1:n.-16-201A>T
ENST00000682764.1:c.-16-201A>T	ENSP00000506780.1:n.-16-201A>T
ENST00000339994.5:c.45A>T MANE Select	ENSP00000345708.4:p.Thr15=
ENST00000339994.4:c.45A>T	ENSP00000345708.4:p.Thr15=
ENST00000526912.1:c.-46A>T	ENSP00000432729.1:n.-46A>T
ENST00000528731.1:c.-16-201A>T	ENSP00000434755.1:n.-16-201A>T
ENST00000528992.1:c.62A>T
NM_000525.3:c.45A>T	NP_000516.3:p.Thr15=
NM_001166290.1:c.-16-201A>T	NP_001159762.1:n.-16-201A>T
XM_006718226.2:c.-16-201A>T	XP_006718289.1:n.-16-201A>T
XR_930867.1:n.203A>T
XM_006718226.3:c.-16-201A>T	XP_006718289.1:n.-16-201A>T
XM_017017680.1:c.-16-201A>T	XP_016873169.1:n.-16-201A>T
NM_001166290.2:c.-16-201A>T	NP_001159762.1:n.-16-201A>T
NM_001377296.1:c.-46A>T	NP_001364225.1:n.-46A>T
NM_001377297.1:c.-16-201A>T	NP_001364226.1:n.-16-201A>T
NM_000525.4:c.45A>T MANE Select	NP_000516.3:p.Thr15=