Canonical Allele Identifier: CA1820664445
Gene: KCNQ3 HGNC NCBI

Linked Data

dbSNP Id: rs1826510283

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132175296_132175297insATA , CM000670.2:g.132175296_132175297insATA GRCh38
NC_000008.10:g.133187543_133187544insATA , CM000670.1:g.133187543_133187544insATA GRCh37
NC_000008.9:g.133256725_133256726insATA NCBI36
NG_008854.2:g.310461_310462insTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000388996.10:c.933+156_933+157insTAT MANE Select ENSP00000373648.3:n.933+156_933+157insTAT
ENST00000521134.6:c.573+156_573+157insTAT ENSP00000429799.1:n.573+156_573+157insTAT
ENST00000638588.1:c.606+156_606+157insTAT ENSP00000491940.1:n.606+156_606+157insTAT
ENST00000639358.1:c.583+156_583+157insTAT
ENST00000639496.1:c.606+156_606+157insTAT ENSP00000491165.1:n.606+156_606+157insTAT
ENST00000388996.8:c.933+156_933+157insTAT ENSP00000373648.3:n.933+156_933+157insTAT
ENST00000519445.5:c.933+156_933+157insTAT ENSP00000428790.1:n.933+156_933+157insTAT
ENST00000519589.1:n.711+156_711+157insTAT
ENST00000521134.5:c.573+156_573+157insTAT ENSP00000429799.1:n.573+156_573+157insTAT
ENST00000621976.1:c.570+156_570+157insTAT ENSP00000482510.1:n.570+156_570+157insTAT
NM_001204824.1:c.573+156_573+157insTAT NP_001191753.1:n.573+156_573+157insTAT
NM_004519.3:c.933+156_933+157insTAT NP_004510.1:n.933+156_933+157insTAT
XM_005250914.2:c.-224+156_-224+157insTAT XP_005250971.1:n.-224+156_-224+157insTAT
XM_006716555.2:c.225+156_225+157insTAT XP_006716618.1:n.225+156_225+157insTAT
XM_011517026.1:c.573+156_573+157insTAT XP_011515328.1:n.573+156_573+157insTAT
XM_005250914.3:c.-224+156_-224+157insTAT XP_005250971.1:n.-224+156_-224+157insTAT
XM_006716555.3:c.225+156_225+157insTAT XP_006716618.1:n.225+156_225+157insTAT
XM_011517026.2:c.573+156_573+157insTAT XP_011515328.1:n.573+156_573+157insTAT
XM_017013400.1:c.711+156_711+157insTAT XP_016868889.1:n.711+156_711+157insTAT
NM_004519.4:c.933+156_933+157insTAT MANE Select NP_004510.1:n.933+156_933+157insTAT
NM_001204824.2:c.573+156_573+157insTAT NP_001191753.1:n.573+156_573+157insTAT