Canonical Allele Identifier: CA1820664030

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132174295G= , CM000670.2:g.132174295G=	GRCh38
NC_000008.10:g.133186542G= , CM000670.1:g.133186542G=	GRCh37
NC_000008.9:g.133255724G=	NCBI36
NG_008854.2:g.311463C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004519.4:c.988C= MANE Select	NP_004510.1:p.Arg330=
ENST00000388996.10:c.988C= MANE Select	ENSP00000373648.3:p.Arg330=
NM_001204824.1:c.628C=	NP_001191753.1:p.Arg210=
NM_001204824.2:c.628C=	NP_001191753.1:p.Arg210=
NM_004519.3:c.988C=	NP_004510.1:p.Arg330=
ENST00000388996.8:c.988C=	ENSP00000373648.3:p.Arg330=
ENST00000519445.5:c.988C=	ENSP00000428790.1:p.Arg330=
ENST00000519589.1:n.766C=
ENST00000521134.5:c.628C=	ENSP00000429799.1:p.Arg210=
ENST00000521134.6:c.628C=	ENSP00000429799.1:p.Arg210=
ENST00000621976.1:c.625C=	ENSP00000482510.1:p.Arg209=
ENST00000638588.1:c.661C=	ENSP00000491940.1:p.Arg221=
ENST00000639358.1:c.638C=
ENST00000639496.1:c.661C=	ENSP00000491165.1:p.Arg221=
XM_005250914.2:c.-169C=	XP_005250971.1:n.-169C=
XM_005250914.3:c.-169C=	XP_005250971.1:n.-169C=
XM_006716555.2:c.280C=	XP_006716618.1:p.Arg94=
XM_006716555.3:c.280C=	XP_006716618.1:p.Arg94=
XM_011517026.1:c.628C=	XP_011515328.1:p.Arg210=
XM_011517026.2:c.628C=	XP_011515328.1:p.Arg210=
XM_017013400.1:c.766C=	XP_016868889.1:p.Arg256=