Canonical Allele Identifier: CA379770815
Gene: KCNJ11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17387314C>A , CM000673.2:g.17387314C>A GRCh38
NC_000011.9:g.17408861C>A , CM000673.1:g.17408861C>A GRCh37
NC_000011.8:g.17365437C>A NCBI36
NG_012446.1:g.6346G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682350.1:c.517G>T ENSP00000508090.1:p.Val173Phe
ENST00000682764.1:c.517G>T ENSP00000506780.1:p.Val173Phe
ENST00000339994.5:c.778G>T MANE Select ENSP00000345708.4:p.Val260Phe
ENST00000339994.4:c.778G>T ENSP00000345708.4:p.Val260Phe
ENST00000528731.1:c.517G>T ENSP00000434755.1:p.Val173Phe
NM_000525.3:c.778G>T NP_000516.3:p.Val260Phe
NM_001166290.1:c.517G>T NP_001159762.1:p.Val173Phe
XM_006718226.2:c.517G>T XP_006718289.1:p.Val173Phe
XR_930867.1:n.936G>T
XM_006718226.3:c.517G>T XP_006718289.1:p.Val173Phe
XM_017017680.1:c.517G>T XP_016873169.1:p.Val173Phe
NM_001166290.2:c.517G>T NP_001159762.1:p.Val173Phe
NM_001377296.1:c.517G>T NP_001364225.1:p.Val173Phe
NM_001377297.1:c.517G>T NP_001364226.1:p.Val173Phe
NM_000525.4:c.778G>T MANE Select NP_000516.3:p.Val260Phe