Canonical Allele Identifier: CA2688627334

Gene: KCNQ3

Linked Data

• gnomAD v4: 8-132175326-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175326_132175327insAA , CM000670.2:g.132175326_132175327insAA	GRCh38
NC_000008.10:g.133187573_133187574insAA , CM000670.1:g.133187573_133187574insAA	GRCh37
NC_000008.9:g.133256755_133256756insAA	NCBI36
NG_008854.2:g.310431_310432insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.933+126_933+127insTT MANE Select	ENSP00000373648.3:n.933+126_933+127insTT
ENST00000521134.6:c.573+126_573+127insTT	ENSP00000429799.1:n.573+126_573+127insTT
ENST00000638588.1:c.606+126_606+127insTT	ENSP00000491940.1:n.606+126_606+127insTT
ENST00000639358.1:c.583+126_583+127insTT
ENST00000639496.1:c.606+126_606+127insTT	ENSP00000491165.1:n.606+126_606+127insTT
ENST00000388996.8:c.933+126_933+127insTT	ENSP00000373648.3:n.933+126_933+127insTT
ENST00000519445.5:c.933+126_933+127insTT	ENSP00000428790.1:n.933+126_933+127insTT
ENST00000519589.1:n.711+126_711+127insTT
ENST00000521134.5:c.573+126_573+127insTT	ENSP00000429799.1:n.573+126_573+127insTT
ENST00000621976.1:c.570+126_570+127insTT	ENSP00000482510.1:n.570+126_570+127insTT
NM_001204824.1:c.573+126_573+127insTT	NP_001191753.1:n.573+126_573+127insTT
NM_004519.3:c.933+126_933+127insTT	NP_004510.1:n.933+126_933+127insTT
XM_005250914.2:c.-224+126_-224+127insTT	XP_005250971.1:n.-224+126_-224+127insTT
XM_006716555.2:c.225+126_225+127insTT	XP_006716618.1:n.225+126_225+127insTT
XM_011517026.1:c.573+126_573+127insTT	XP_011515328.1:n.573+126_573+127insTT
XM_005250914.3:c.-224+126_-224+127insTT	XP_005250971.1:n.-224+126_-224+127insTT
XM_006716555.3:c.225+126_225+127insTT	XP_006716618.1:n.225+126_225+127insTT
XM_011517026.2:c.573+126_573+127insTT	XP_011515328.1:n.573+126_573+127insTT
XM_017013400.1:c.711+126_711+127insTT	XP_016868889.1:n.711+126_711+127insTT
NM_004519.4:c.933+126_933+127insTT MANE Select	NP_004510.1:n.933+126_933+127insTT
NM_001204824.2:c.573+126_573+127insTT	NP_001191753.1:n.573+126_573+127insTT