Canonical Allele Identifier: CA1820653864

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132134369G= , CM000670.2:g.132134369G=	GRCh38
NC_000008.10:g.133146616G= , CM000670.1:g.133146616G=	GRCh37
NC_000008.9:g.133215798G=	NCBI36
NG_008854.2:g.351389C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.1720C= MANE Select	ENSP00000373648.3:p.Pro574=
ENST00000521134.6:c.1360C=	ENSP00000429799.1:p.Pro454=
ENST00000638588.1:c.1393C=	ENSP00000491940.1:p.Pro465=
ENST00000639496.1:c.*344C=	ENSP00000491165.1:n.*344C=
ENST00000388996.8:c.1720C=	ENSP00000373648.3:p.Pro574=
ENST00000519445.5:c.1720C=	ENSP00000428790.1:p.Pro574=
ENST00000519589.1:n.2448C=
ENST00000521134.5:c.1360C=	ENSP00000429799.1:p.Pro454=
ENST00000621976.1:c.1357C=	ENSP00000482510.1:p.Pro453=
NM_001204824.1:c.1360C=	NP_001191753.1:p.Pro454=
NM_004519.3:c.1720C=	NP_004510.1:p.Pro574=
XM_005250914.2:c.475C=	XP_005250971.1:p.Pro159=
XM_006716555.2:c.1012C=	XP_006716618.1:p.Pro338=
XM_011517026.1:c.1360C=	XP_011515328.1:p.Pro454=
XM_005250914.3:c.475C=	XP_005250971.1:p.Pro159=
XM_006716555.3:c.1012C=	XP_006716618.1:p.Pro338=
XM_011517026.2:c.1360C=	XP_011515328.1:p.Pro454=
XM_017013400.1:c.1498C=	XP_016868889.1:p.Pro500=
NM_004519.4:c.1720C= MANE Select	NP_004510.1:p.Pro574=
NM_001204824.2:c.1360C=	NP_001191753.1:p.Pro454=