Canonical Allele Identifier: CA1820664523
Gene: KCNQ3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132175474T= , CM000670.2:g.132175474T= GRCh38
NC_000008.10:g.133187721T= , CM000670.1:g.133187721T= GRCh37
NC_000008.9:g.133256903T= NCBI36
NG_008854.2:g.310284A=

Transcript Alleles

HGVS Amino-acid change
ENST00000388996.10:c.912A= MANE Select ENSP00000373648.3:p.Ala304=
ENST00000521134.6:c.552A= ENSP00000429799.1:p.Ala184=
ENST00000638588.1:c.585A= ENSP00000491940.1:p.Ala195=
ENST00000639358.1:c.562A=
ENST00000639496.1:c.585A= ENSP00000491165.1:p.Ala195=
ENST00000388996.8:c.912A= ENSP00000373648.3:p.Ala304=
ENST00000519445.5:c.912A= ENSP00000428790.1:p.Ala304=
ENST00000519589.1:n.690A=
ENST00000521134.5:c.552A= ENSP00000429799.1:p.Ala184=
ENST00000621976.1:c.549A= ENSP00000482510.1:p.Ala183=
NM_001204824.1:c.552A= NP_001191753.1:p.Ala184=
NM_004519.3:c.912A= NP_004510.1:p.Ala304=
XM_005250914.2:c.-245A= XP_005250971.1:n.-245A=
XM_006716555.2:c.204A= XP_006716618.1:p.Ala68=
XM_011517026.1:c.552A= XP_011515328.1:p.Ala184=
XM_005250914.3:c.-245A= XP_005250971.1:n.-245A=
XM_006716555.3:c.204A= XP_006716618.1:p.Ala68=
XM_011517026.2:c.552A= XP_011515328.1:p.Ala184=
XM_017013400.1:c.690A= XP_016868889.1:p.Ala230=
NM_004519.4:c.912A= MANE Select NP_004510.1:p.Ala304=
NM_001204824.2:c.552A= NP_001191753.1:p.Ala184=