Canonical Allele Identifier: CA218398932

Gene: KCNJ11

Linked Data

• dbSNP Id: rs914215053
• gnomAD v2: 11-17408429-T-G
• gnomAD v3: 11-17386882-T-G
• gnomAD v4: 11-17386882-T-G
• MyVariant Identifiers: chr11:g.17408429T>G (hg19) ; chr11:g.17386882T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17386882T>G , CM000673.2:g.17386882T>G	GRCh38
NC_000011.9:g.17408429T>G , CM000673.1:g.17408429T>G	GRCh37
NC_000011.8:g.17365005T>G	NCBI36
NG_012446.1:g.6778A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.*37A>C	ENSP00000508090.1:n.*37A>C
ENST00000682764.1:c.*37A>C	ENSP00000506780.1:n.*37A>C
ENST00000339994.5:c.*37A>C MANE Select	ENSP00000345708.4:n.*37A>C
ENST00000339994.4:c.*37A>C	ENSP00000345708.4:n.*37A>C
ENST00000528731.1:c.*37A>C	ENSP00000434755.1:n.*37A>C
NM_000525.3:c.*37A>C	NP_000516.3:n.*37A>C
NM_001166290.1:c.*37A>C	NP_001159762.1:n.*37A>C
XM_006718226.2:c.*37A>C	XP_006718289.1:n.*37A>C
XR_930867.1:n.1368A>C
XM_006718226.3:c.*37A>C	XP_006718289.1:n.*37A>C
XM_017017680.1:c.*37A>C	XP_016873169.1:n.*37A>C
NM_001166290.2:c.*37A>C	NP_001159762.1:n.*37A>C
NM_001377296.1:c.*37A>C	NP_001364225.1:n.*37A>C
NM_001377297.1:c.*37A>C	NP_001364226.1:n.*37A>C
NM_000525.4:c.*37A>C MANE Select	NP_000516.3:n.*37A>C