Canonical Allele Identifier: CA473515437
Gene: KCNJ11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.17409057G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387510G>T , CM000673.2:g.17387510G>T GRCh38
NC_000011.9:g.17409057G>T , CM000673.1:g.17409057G>T GRCh37
NC_000011.8:g.17365633G>T NCBI36
NG_012446.1:g.6150C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000682350.1:c.321C>A ENSP00000508090.1:p.Gly107=
ENST00000682764.1:c.321C>A ENSP00000506780.1:p.Gly107=
ENST00000339994.5:c.582C>A MANE Select ENSP00000345708.4:p.Gly194=
ENST00000339994.4:c.582C>A ENSP00000345708.4:p.Gly194=
ENST00000526912.1:c.321C>A ENSP00000432729.1:p.Gly107=
ENST00000528731.1:c.321C>A ENSP00000434755.1:p.Gly107=
NM_000525.3:c.582C>A NP_000516.3:p.Gly194=
NM_001166290.1:c.321C>A NP_001159762.1:p.Gly107=
XM_006718226.2:c.321C>A XP_006718289.1:p.Gly107=
XR_930867.1:n.740C>A
XM_006718226.3:c.321C>A XP_006718289.1:p.Gly107=
XM_017017680.1:c.321C>A XP_016873169.1:p.Gly107=
NM_001166290.2:c.321C>A NP_001159762.1:p.Gly107=
NM_001377296.1:c.321C>A NP_001364225.1:p.Gly107=
NM_001377297.1:c.321C>A NP_001364226.1:p.Gly107=
NM_000525.4:c.582C>A MANE Select NP_000516.3:p.Gly194=