Canonical Allele Identifier: CA372290335
Gene: KCNQ3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132175475G>C , CM000670.2:g.132175475G>C GRCh38
NC_000008.10:g.133187722G>C , CM000670.1:g.133187722G>C GRCh37
NC_000008.9:g.133256904G>C NCBI36
NG_008854.2:g.310283C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000388996.10:c.911C>G MANE Select ENSP00000373648.3:p.Ala304Gly
ENST00000521134.6:c.551C>G ENSP00000429799.1:p.Ala184Gly
ENST00000638588.1:c.584C>G ENSP00000491940.1:p.Ala195Gly
ENST00000639358.1:c.561C>G
ENST00000639496.1:c.584C>G ENSP00000491165.1:p.Ala195Gly
ENST00000388996.8:c.911C>G ENSP00000373648.3:p.Ala304Gly
ENST00000519445.5:c.911C>G ENSP00000428790.1:p.Ala304Gly
ENST00000519589.1:n.689C>G
ENST00000521134.5:c.551C>G ENSP00000429799.1:p.Ala184Gly
ENST00000621976.1:c.548C>G ENSP00000482510.1:p.Ala183Gly
NM_001204824.1:c.551C>G NP_001191753.1:p.Ala184Gly
NM_004519.3:c.911C>G NP_004510.1:p.Ala304Gly
XM_005250914.2:c.-246C>G XP_005250971.1:n.-246C>G
XM_006716555.2:c.203C>G XP_006716618.1:p.Ala68Gly
XM_011517026.1:c.551C>G XP_011515328.1:p.Ala184Gly
XM_005250914.3:c.-246C>G XP_005250971.1:n.-246C>G
XM_006716555.3:c.203C>G XP_006716618.1:p.Ala68Gly
XM_011517026.2:c.551C>G XP_011515328.1:p.Ala184Gly
XM_017013400.1:c.689C>G XP_016868889.1:p.Ala230Gly
NM_004519.4:c.911C>G MANE Select NP_004510.1:p.Ala304Gly
NM_001204824.2:c.551C>G NP_001191753.1:p.Ala184Gly