Canonical Allele Identifier: CA2782246973
Gene: KCNQ3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132175683_132175684insAACACACCCAACACA , CM000670.2:g.132175683_132175684insAACACACCCAACACA GRCh38
NC_000008.10:g.133187930_133187931insAACACACCCAACACA , CM000670.1:g.133187930_133187931insAACACACCCAACACA GRCh37
NC_000008.9:g.133257112_133257113insAACACACCCAACACA NCBI36
NG_008854.2:g.310076_310077insTGTTGGGTGTGTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000388996.10:c.778-74_778-73insTGTTGGGTGTGTTTG MANE Select ENSP00000373648.3:n.778-74_778-73insTGTTGGGTGTGTTTG
ENST00000521134.6:c.418-74_418-73insTGTTGGGTGTGTTTG ENSP00000429799.1:n.418-74_418-73insTGTTGGGTGTGTTTG
ENST00000638588.1:c.451-74_451-73insTGTTGGGTGTGTTTG ENSP00000491940.1:n.451-74_451-73insTGTTGGGTGTGTTTG
ENST00000639358.1:c.428-74_428-73insTGTTGGGTGTGTTTG
ENST00000639496.1:c.451-74_451-73insTGTTGGGTGTGTTTG ENSP00000491165.1:n.451-74_451-73insTGTTGGGTGTGTTTG
ENST00000388996.8:c.778-74_778-73insTGTTGGGTGTGTTTG ENSP00000373648.3:n.778-74_778-73insTGTTGGGTGTGTTTG
ENST00000519445.5:c.778-74_778-73insTGTTGGGTGTGTTTG ENSP00000428790.1:n.778-74_778-73insTGTTGGGTGTGTTTG
ENST00000519589.1:n.556-74_556-73insTGTTGGGTGTGTTTG
ENST00000521134.5:c.418-74_418-73insTGTTGGGTGTGTTTG ENSP00000429799.1:n.418-74_418-73insTGTTGGGTGTGTTTG
ENST00000621976.1:c.415-74_415-73insTGTTGGGTGTGTTTG ENSP00000482510.1:n.415-74_415-73insTGTTGGGTGTGTTTG
NM_001204824.1:c.418-74_418-73insTGTTGGGTGTGTTTG NP_001191753.1:n.418-74_418-73insTGTTGGGTGTGTTTG
NM_004519.3:c.778-74_778-73insTGTTGGGTGTGTTTG NP_004510.1:n.778-74_778-73insTGTTGGGTGTGTTTG
XM_005250914.2:c.-379-74_-379-73insTGTTGGGTGTGTTTG XP_005250971.1:n.-379-74_-379-73insTGTTGGGTGTGTTTG
XM_006716555.2:c.70-74_70-73insTGTTGGGTGTGTTTG XP_006716618.1:n.70-74_70-73insTGTTGGGTGTGTTTG
XM_011517026.1:c.418-74_418-73insTGTTGGGTGTGTTTG XP_011515328.1:n.418-74_418-73insTGTTGGGTGTGTTTG
XM_005250914.3:c.-379-74_-379-73insTGTTGGGTGTGTTTG XP_005250971.1:n.-379-74_-379-73insTGTTGGGTGTGTTTG
XM_006716555.3:c.70-74_70-73insTGTTGGGTGTGTTTG XP_006716618.1:n.70-74_70-73insTGTTGGGTGTGTTTG
XM_011517026.2:c.418-74_418-73insTGTTGGGTGTGTTTG XP_011515328.1:n.418-74_418-73insTGTTGGGTGTGTTTG
XM_017013400.1:c.556-74_556-73insTGTTGGGTGTGTTTG XP_016868889.1:n.556-74_556-73insTGTTGGGTGTGTTTG
NM_004519.4:c.778-74_778-73insTGTTGGGTGTGTTTG MANE Select NP_004510.1:n.778-74_778-73insTGTTGGGTGTGTTTG
NM_001204824.2:c.418-74_418-73insTGTTGGGTGTGTTTG NP_001191753.1:n.418-74_418-73insTGTTGGGTGTGTTTG