Canonical Allele Identifier: CA463070251

Gene: KCNQ3

Linked Data

• gnomAD v4: 8-132174239-C-A
• MyVariant Identifiers: chr8:g.133186486C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132174239C>A , CM000670.2:g.132174239C>A	GRCh38
NC_000008.10:g.133186486C>A , CM000670.1:g.133186486C>A	GRCh37
NC_000008.9:g.133255668C>A	NCBI36
NG_008854.2:g.311519G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.1044G>T MANE Select	ENSP00000373648.3:p.Ala348=
ENST00000521134.6:c.684G>T	ENSP00000429799.1:p.Ala228=
ENST00000638588.1:c.717G>T	ENSP00000491940.1:p.Ala239=
ENST00000639358.1:c.694G>T
ENST00000639496.1:c.717G>T	ENSP00000491165.1:p.Ala239=
ENST00000388996.8:c.1044G>T	ENSP00000373648.3:p.Ala348=
ENST00000519445.5:c.1044G>T	ENSP00000428790.1:p.Ala348=
ENST00000519589.1:n.822G>T
ENST00000521134.5:c.684G>T	ENSP00000429799.1:p.Ala228=
ENST00000621976.1:c.681G>T	ENSP00000482510.1:p.Ala227=
NM_001204824.1:c.684G>T	NP_001191753.1:p.Ala228=
NM_004519.3:c.1044G>T	NP_004510.1:p.Ala348=
XM_005250914.2:c.-113G>T	XP_005250971.1:n.-113G>T
XM_006716555.2:c.336G>T	XP_006716618.1:p.Ala112=
XM_011517026.1:c.684G>T	XP_011515328.1:p.Ala228=
XM_005250914.3:c.-113G>T	XP_005250971.1:n.-113G>T
XM_006716555.3:c.336G>T	XP_006716618.1:p.Ala112=
XM_011517026.2:c.684G>T	XP_011515328.1:p.Ala228=
XM_017013400.1:c.822G>T	XP_016868889.1:p.Ala274=
NM_004519.4:c.1044G>T MANE Select	NP_004510.1:p.Ala348=
NM_001204824.2:c.684G>T	NP_001191753.1:p.Ala228=