Canonical Allele Identifier: CA473515728

Gene: KCNJ11

Linked Data

• dbSNP Id: rs746264957
• MyVariant Identifiers: chr11:g.17409594T>G (hg19)

Genomic Alleles

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

Transcript Alleles

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