Canonical Allele Identifier: CA1820664031
Gene: KCNQ3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132174298C= , CM000670.2:g.132174298C= GRCh38
NC_000008.10:g.133186545C= , CM000670.1:g.133186545C= GRCh37
NC_000008.9:g.133255727C= NCBI36
NG_008854.2:g.311460G=

Transcript Alleles

HGVS Amino-acid change
ENST00000388996.10:c.985G= MANE Select ENSP00000373648.3:p.Gly329=
ENST00000521134.6:c.625G= ENSP00000429799.1:p.Gly209=
ENST00000638588.1:c.658G= ENSP00000491940.1:p.Gly220=
ENST00000639358.1:c.635G=
ENST00000639496.1:c.658G= ENSP00000491165.1:p.Gly220=
ENST00000388996.8:c.985G= ENSP00000373648.3:p.Gly329=
ENST00000519445.5:c.985G= ENSP00000428790.1:p.Gly329=
ENST00000519589.1:n.763G=
ENST00000521134.5:c.625G= ENSP00000429799.1:p.Gly209=
ENST00000621976.1:c.622G= ENSP00000482510.1:p.Gly208=
NM_001204824.1:c.625G= NP_001191753.1:p.Gly209=
NM_004519.3:c.985G= NP_004510.1:p.Gly329=
XM_005250914.2:c.-172G= XP_005250971.1:n.-172G=
XM_006716555.2:c.277G= XP_006716618.1:p.Gly93=
XM_011517026.1:c.625G= XP_011515328.1:p.Gly209=
XM_005250914.3:c.-172G= XP_005250971.1:n.-172G=
XM_006716555.3:c.277G= XP_006716618.1:p.Gly93=
XM_011517026.2:c.625G= XP_011515328.1:p.Gly209=
XM_017013400.1:c.763G= XP_016868889.1:p.Gly255=
NM_004519.4:c.985G= MANE Select NP_004510.1:p.Gly329=
NM_001204824.2:c.625G= NP_001191753.1:p.Gly209=