Canonical Allele Identifier: CA372290216
Gene: KCNQ3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132174320G>T , CM000670.2:g.132174320G>T GRCh38
NC_000008.10:g.133186567G>T , CM000670.1:g.133186567G>T GRCh37
NC_000008.9:g.133255749G>T NCBI36
NG_008854.2:g.311438C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000388996.10:c.963C>A MANE Select ENSP00000373648.3:p.Asp321Glu
ENST00000521134.6:c.603C>A ENSP00000429799.1:p.Asp201Glu
ENST00000638588.1:c.636C>A ENSP00000491940.1:p.Asp212Glu
ENST00000639358.1:c.613C>A
ENST00000639496.1:c.636C>A ENSP00000491165.1:p.Asp212Glu
ENST00000388996.8:c.963C>A ENSP00000373648.3:p.Asp321Glu
ENST00000519445.5:c.963C>A ENSP00000428790.1:p.Asp321Glu
ENST00000519589.1:n.741C>A
ENST00000521134.5:c.603C>A ENSP00000429799.1:p.Asp201Glu
ENST00000621976.1:c.600C>A ENSP00000482510.1:p.Asp200Glu
NM_001204824.1:c.603C>A NP_001191753.1:p.Asp201Glu
NM_004519.3:c.963C>A NP_004510.1:p.Asp321Glu
XM_005250914.2:c.-194C>A XP_005250971.1:n.-194C>A
XM_006716555.2:c.255C>A XP_006716618.1:p.Asp85Glu
XM_011517026.1:c.603C>A XP_011515328.1:p.Asp201Glu
XM_005250914.3:c.-194C>A XP_005250971.1:n.-194C>A
XM_006716555.3:c.255C>A XP_006716618.1:p.Asp85Glu
XM_011517026.2:c.603C>A XP_011515328.1:p.Asp201Glu
XM_017013400.1:c.741C>A XP_016868889.1:p.Asp247Glu
NM_004519.4:c.963C>A MANE Select NP_004510.1:p.Asp321Glu
NM_001204824.2:c.603C>A NP_001191753.1:p.Asp201Glu