Canonical Allele Identifier: CA1820664029

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132174294C= , CM000670.2:g.132174294C=	GRCh38
NC_000008.10:g.133186541C= , CM000670.1:g.133186541C=	GRCh37
NC_000008.9:g.133255723C=	NCBI36
NG_008854.2:g.311464G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.989G= MANE Select	ENSP00000373648.3:p.Arg330=
ENST00000521134.6:c.629G=	ENSP00000429799.1:p.Arg210=
ENST00000638588.1:c.662G=	ENSP00000491940.1:p.Arg221=
ENST00000639358.1:c.639G=
ENST00000639496.1:c.662G=	ENSP00000491165.1:p.Arg221=
ENST00000388996.8:c.989G=	ENSP00000373648.3:p.Arg330=
ENST00000519445.5:c.989G=	ENSP00000428790.1:p.Arg330=
ENST00000519589.1:n.767G=
ENST00000521134.5:c.629G=	ENSP00000429799.1:p.Arg210=
ENST00000621976.1:c.626G=	ENSP00000482510.1:p.Arg209=
NM_001204824.1:c.629G=	NP_001191753.1:p.Arg210=
NM_004519.3:c.989G=	NP_004510.1:p.Arg330=
XM_005250914.2:c.-168G=	XP_005250971.1:n.-168G=
XM_006716555.2:c.281G=	XP_006716618.1:p.Arg94=
XM_011517026.1:c.629G=	XP_011515328.1:p.Arg210=
XM_005250914.3:c.-168G=	XP_005250971.1:n.-168G=
XM_006716555.3:c.281G=	XP_006716618.1:p.Arg94=
XM_011517026.2:c.629G=	XP_011515328.1:p.Arg210=
XM_017013400.1:c.767G=	XP_016868889.1:p.Arg256=
NM_004519.4:c.989G= MANE Select	NP_004510.1:p.Arg330=
NM_001204824.2:c.629G=	NP_001191753.1:p.Arg210=