Canonical Allele Identifier: CA2688627322

Gene: KCNQ3

Linked Data

• gnomAD v4: 8-132175314-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175314T>C , CM000670.2:g.132175314T>C	GRCh38
NC_000008.10:g.133187561T>C , CM000670.1:g.133187561T>C	GRCh37
NC_000008.9:g.133256743T>C	NCBI36
NG_008854.2:g.310444A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.933+139A>G MANE Select	ENSP00000373648.3:n.933+139A>G
ENST00000521134.6:c.573+139A>G	ENSP00000429799.1:n.573+139A>G
ENST00000638588.1:c.606+139A>G	ENSP00000491940.1:n.606+139A>G
ENST00000639358.1:c.583+139A>G
ENST00000639496.1:c.606+139A>G	ENSP00000491165.1:n.606+139A>G
ENST00000388996.8:c.933+139A>G	ENSP00000373648.3:n.933+139A>G
ENST00000519445.5:c.933+139A>G	ENSP00000428790.1:n.933+139A>G
ENST00000519589.1:n.711+139A>G
ENST00000521134.5:c.573+139A>G	ENSP00000429799.1:n.573+139A>G
ENST00000621976.1:c.570+139A>G	ENSP00000482510.1:n.570+139A>G
NM_001204824.1:c.573+139A>G	NP_001191753.1:n.573+139A>G
NM_004519.3:c.933+139A>G	NP_004510.1:n.933+139A>G
XM_005250914.2:c.-224+139A>G	XP_005250971.1:n.-224+139A>G
XM_006716555.2:c.225+139A>G	XP_006716618.1:n.225+139A>G
XM_011517026.1:c.573+139A>G	XP_011515328.1:n.573+139A>G
XM_005250914.3:c.-224+139A>G	XP_005250971.1:n.-224+139A>G
XM_006716555.3:c.225+139A>G	XP_006716618.1:n.225+139A>G
XM_011517026.2:c.573+139A>G	XP_011515328.1:n.573+139A>G
XM_017013400.1:c.711+139A>G	XP_016868889.1:n.711+139A>G
NM_004519.4:c.933+139A>G MANE Select	NP_004510.1:n.933+139A>G
NM_001204824.2:c.573+139A>G	NP_001191753.1:n.573+139A>G