Canonical Allele Identifier: CA1955119183
Gene: KCNJ11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387252G= , CM000673.2:g.17387252G= GRCh38
NC_000011.9:g.17408799G= , CM000673.1:g.17408799G= GRCh37
NC_000011.8:g.17365375G= NCBI36
NG_012446.1:g.6408C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682350.1:c.579C= ENSP00000508090.1:p.Asp193=
ENST00000682764.1:c.579C= ENSP00000506780.1:p.Asp193=
ENST00000339994.5:c.840C= MANE Select ENSP00000345708.4:p.Asp280=
ENST00000339994.4:c.840C= ENSP00000345708.4:p.Asp280=
ENST00000528731.1:c.579C= ENSP00000434755.1:p.Asp193=
NM_000525.3:c.840C= NP_000516.3:p.Asp280=
NM_001166290.1:c.579C= NP_001159762.1:p.Asp193=
XM_006718226.2:c.579C= XP_006718289.1:p.Asp193=
XR_930867.1:n.998C=
XM_006718226.3:c.579C= XP_006718289.1:p.Asp193=
XM_017017680.1:c.579C= XP_016873169.1:p.Asp193=
NM_001166290.2:c.579C= NP_001159762.1:p.Asp193=
NM_001377296.1:c.579C= NP_001364225.1:p.Asp193=
NM_001377297.1:c.579C= NP_001364226.1:p.Asp193=
NM_000525.4:c.840C= MANE Select NP_000516.3:p.Asp280=