Canonical Allele Identifier: CA379770242

Gene: KCNJ11

Linked Data

• MyVariant Identifiers: chr11:g.17408781G>C (hg19) ; chr11:g.17387234G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17387234G>C , CM000673.2:g.17387234G>C	GRCh38
NC_000011.9:g.17408781G>C , CM000673.1:g.17408781G>C	GRCh37
NC_000011.8:g.17365357G>C	NCBI36
NG_012446.1:g.6426C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682350.1:c.597C>G	ENSP00000508090.1:p.Ile199Met
ENST00000682764.1:c.597C>G	ENSP00000506780.1:p.Ile199Met
ENST00000339994.5:c.858C>G MANE Select	ENSP00000345708.4:p.Ile286Met
ENST00000339994.4:c.858C>G	ENSP00000345708.4:p.Ile286Met
ENST00000528731.1:c.597C>G	ENSP00000434755.1:p.Ile199Met
NM_000525.3:c.858C>G	NP_000516.3:p.Ile286Met
NM_001166290.1:c.597C>G	NP_001159762.1:p.Ile199Met
XM_006718226.2:c.597C>G	XP_006718289.1:p.Ile199Met
XR_930867.1:n.1016C>G
XM_006718226.3:c.597C>G	XP_006718289.1:p.Ile199Met
XM_017017680.1:c.597C>G	XP_016873169.1:p.Ile199Met
NM_001166290.2:c.597C>G	NP_001159762.1:p.Ile199Met
NM_001377296.1:c.597C>G	NP_001364225.1:p.Ile199Met
NM_001377297.1:c.597C>G	NP_001364226.1:p.Ile199Met
NM_000525.4:c.858C>G MANE Select	NP_000516.3:p.Ile286Met