Canonical Allele Identifier: CA1820664033
Gene: KCNQ3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132174306G= , CM000670.2:g.132174306G= GRCh38
NC_000008.10:g.133186553G= , CM000670.1:g.133186553G= GRCh37
NC_000008.9:g.133255735G= NCBI36
NG_008854.2:g.311452C=

Transcript Alleles

HGVS Amino-acid change
ENST00000388996.10:c.977C= MANE Select ENSP00000373648.3:p.Thr326=
ENST00000521134.6:c.617C= ENSP00000429799.1:p.Thr206=
ENST00000638588.1:c.650C= ENSP00000491940.1:p.Thr217=
ENST00000639358.1:c.627C=
ENST00000639496.1:c.650C= ENSP00000491165.1:p.Thr217=
ENST00000388996.8:c.977C= ENSP00000373648.3:p.Thr326=
ENST00000519445.5:c.977C= ENSP00000428790.1:p.Thr326=
ENST00000519589.1:n.755C=
ENST00000521134.5:c.617C= ENSP00000429799.1:p.Thr206=
ENST00000621976.1:c.614C= ENSP00000482510.1:p.Thr205=
NM_001204824.1:c.617C= NP_001191753.1:p.Thr206=
NM_004519.3:c.977C= NP_004510.1:p.Thr326=
XM_005250914.2:c.-180C= XP_005250971.1:n.-180C=
XM_006716555.2:c.269C= XP_006716618.1:p.Thr90=
XM_011517026.1:c.617C= XP_011515328.1:p.Thr206=
XM_005250914.3:c.-180C= XP_005250971.1:n.-180C=
XM_006716555.3:c.269C= XP_006716618.1:p.Thr90=
XM_011517026.2:c.617C= XP_011515328.1:p.Thr206=
XM_017013400.1:c.755C= XP_016868889.1:p.Thr252=
NM_004519.4:c.977C= MANE Select NP_004510.1:p.Thr326=
NM_001204824.2:c.617C= NP_001191753.1:p.Thr206=