Canonical Allele Identifier: CA1820664522
Gene: KCNQ3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132175473C= , CM000670.2:g.132175473C= GRCh38
NC_000008.10:g.133187720C= , CM000670.1:g.133187720C= GRCh37
NC_000008.9:g.133256902C= NCBI36
NG_008854.2:g.310285G=

Transcript Alleles

HGVS Amino-acid change
ENST00000388996.10:c.913G= MANE Select ENSP00000373648.3:p.Asp305=
ENST00000521134.6:c.553G= ENSP00000429799.1:p.Asp185=
ENST00000638588.1:c.586G= ENSP00000491940.1:p.Asp196=
ENST00000639358.1:c.563G=
ENST00000639496.1:c.586G= ENSP00000491165.1:p.Asp196=
ENST00000388996.8:c.913G= ENSP00000373648.3:p.Asp305=
ENST00000519445.5:c.913G= ENSP00000428790.1:p.Asp305=
ENST00000519589.1:n.691G=
ENST00000521134.5:c.553G= ENSP00000429799.1:p.Asp185=
ENST00000621976.1:c.550G= ENSP00000482510.1:p.Asp184=
NM_001204824.1:c.553G= NP_001191753.1:p.Asp185=
NM_004519.3:c.913G= NP_004510.1:p.Asp305=
XM_005250914.2:c.-244G= XP_005250971.1:n.-244G=
XM_006716555.2:c.205G= XP_006716618.1:p.Asp69=
XM_011517026.1:c.553G= XP_011515328.1:p.Asp185=
XM_005250914.3:c.-244G= XP_005250971.1:n.-244G=
XM_006716555.3:c.205G= XP_006716618.1:p.Asp69=
XM_011517026.2:c.553G= XP_011515328.1:p.Asp185=
XM_017013400.1:c.691G= XP_016868889.1:p.Asp231=
NM_004519.4:c.913G= MANE Select NP_004510.1:p.Asp305=
NM_001204824.2:c.553G= NP_001191753.1:p.Asp185=