Canonical Allele Identifier: CA1820664535

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175503C= , CM000670.2:g.132175503C=	GRCh38
NC_000008.10:g.133187750C= , CM000670.1:g.133187750C=	GRCh37
NC_000008.9:g.133256932C=	NCBI36
NG_008854.2:g.310255G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000388996.10:c.883G= MANE Select	ENSP00000373648.3:p.Glu295=
ENST00000521134.6:c.523G=	ENSP00000429799.1:p.Glu175=
ENST00000638588.1:c.556G=	ENSP00000491940.1:p.Glu186=
ENST00000639358.1:c.533G=
ENST00000639496.1:c.556G=	ENSP00000491165.1:p.Glu186=
ENST00000388996.8:c.883G=	ENSP00000373648.3:p.Glu295=
ENST00000519445.5:c.883G=	ENSP00000428790.1:p.Glu295=
ENST00000519589.1:n.661G=
ENST00000521134.5:c.523G=	ENSP00000429799.1:p.Glu175=
ENST00000621976.1:c.520G=	ENSP00000482510.1:p.Glu174=
NM_001204824.1:c.523G=	NP_001191753.1:p.Glu175=
NM_004519.3:c.883G=	NP_004510.1:p.Glu295=
XM_005250914.2:c.-274G=	XP_005250971.1:n.-274G=
XM_006716555.2:c.175G=	XP_006716618.1:p.Glu59=
XM_011517026.1:c.523G=	XP_011515328.1:p.Glu175=
XM_005250914.3:c.-274G=	XP_005250971.1:n.-274G=
XM_006716555.3:c.175G=	XP_006716618.1:p.Glu59=
XM_011517026.2:c.523G=	XP_011515328.1:p.Glu175=
XM_017013400.1:c.661G=	XP_016868889.1:p.Glu221=
NM_004519.4:c.883G= MANE Select	NP_004510.1:p.Glu295=
NM_001204824.2:c.523G=	NP_001191753.1:p.Glu175=