Canonical Allele Identifier: CA1820664532
Gene: KCNQ3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132175497T= , CM000670.2:g.132175497T= GRCh38
NC_000008.10:g.133187744T= , CM000670.1:g.133187744T= GRCh37
NC_000008.9:g.133256926T= NCBI36
NG_008854.2:g.310261A=

Transcript Alleles

HGVS Amino-acid change
ENST00000388996.10:c.889A= MANE Select ENSP00000373648.3:p.Lys297=
ENST00000521134.6:c.529A= ENSP00000429799.1:p.Lys177=
ENST00000638588.1:c.562A= ENSP00000491940.1:p.Lys188=
ENST00000639358.1:c.539A=
ENST00000639496.1:c.562A= ENSP00000491165.1:p.Lys188=
ENST00000388996.8:c.889A= ENSP00000373648.3:p.Lys297=
ENST00000519445.5:c.889A= ENSP00000428790.1:p.Lys297=
ENST00000519589.1:n.667A=
ENST00000521134.5:c.529A= ENSP00000429799.1:p.Lys177=
ENST00000621976.1:c.526A= ENSP00000482510.1:p.Lys176=
NM_001204824.1:c.529A= NP_001191753.1:p.Lys177=
NM_004519.3:c.889A= NP_004510.1:p.Lys297=
XM_005250914.2:c.-268A= XP_005250971.1:n.-268A=
XM_006716555.2:c.181A= XP_006716618.1:p.Lys61=
XM_011517026.1:c.529A= XP_011515328.1:p.Lys177=
XM_005250914.3:c.-268A= XP_005250971.1:n.-268A=
XM_006716555.3:c.181A= XP_006716618.1:p.Lys61=
XM_011517026.2:c.529A= XP_011515328.1:p.Lys177=
XM_017013400.1:c.667A= XP_016868889.1:p.Lys223=
NM_004519.4:c.889A= MANE Select NP_004510.1:p.Lys297=
NM_001204824.2:c.529A= NP_001191753.1:p.Lys177=