Canonical Allele Identifier: CA473515669
Gene: KCNJ11 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.17408989del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387442del , CM000673.2:g.17387442del GRCh38
NC_000011.9:g.17408989del , CM000673.1:g.17408989del GRCh37
NC_000011.8:g.17365565del NCBI36
NG_012446.1:g.6218del

Transcript Alleles

HGVS Amino-acid change
ENST00000682350.1:c.389del ENSP00000508090.1:p.Met130SerfsTer?
ENST00000682764.1:c.389del ENSP00000506780.1:p.Met130SerfsTer?
ENST00000339994.5:c.650del MANE Select ENSP00000345708.4:p.Met217SerfsTer?
ENST00000339994.4:c.650del ENSP00000345708.4:p.Met217SerfsTer?
ENST00000526912.1:c.389del ENSP00000432729.1:p.Met130SerfsTer?
ENST00000528731.1:c.389del ENSP00000434755.1:p.Met130SerfsTer?
NM_000525.3:c.650del NP_000516.3:p.Met217SerfsTer?
NM_001166290.1:c.389del NP_001159762.1:p.Met130SerfsTer?
XM_006718226.2:c.389del XP_006718289.1:p.Met130SerfsTer?
XR_930867.1:n.808del
XM_006718226.3:c.389del XP_006718289.1:p.Met130SerfsTer?
XM_017017680.1:c.389del XP_016873169.1:p.Met130SerfsTer?
NM_001166290.2:c.389del NP_001159762.1:p.Met130SerfsTer?
NM_001377296.1:c.389del NP_001364225.1:p.Met130SerfsTer?
NM_001377297.1:c.389del NP_001364226.1:p.Met130SerfsTer?
NM_000525.4:c.650del MANE Select NP_000516.3:p.Met217SerfsTer?