Canonical Allele Identifier: CA1820633230

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132141191T= , CM000670.2:g.132141191T=	GRCh38
NC_000008.10:g.133153438T= , CM000670.1:g.133153438T=	GRCh37
NC_000008.9:g.133222620T=	NCBI36
NG_008854.2:g.344567A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.1403A= MANE Select	ENSP00000373648.3:p.Asn468=
ENST00000521134.6:c.1043A=	ENSP00000429799.1:p.Asn348=
ENST00000638588.1:c.1076A=	ENSP00000491940.1:p.Asn359=
ENST00000639496.1:c.*27A=	ENSP00000491165.1:n.*27A=
ENST00000388996.8:c.1403A=	ENSP00000373648.3:p.Asn468=
ENST00000519445.5:c.1403A=	ENSP00000428790.1:p.Asn468=
ENST00000519589.1:n.1181A=
ENST00000521134.5:c.1043A=	ENSP00000429799.1:p.Asn348=
ENST00000621976.1:c.1040A=	ENSP00000482510.1:p.Asn347=
NM_001204824.1:c.1043A=	NP_001191753.1:p.Asn348=
NM_004519.3:c.1403A=	NP_004510.1:p.Asn468=
XM_005250914.2:c.158A=	XP_005250971.1:p.Asn53=
XM_006716555.2:c.695A=	XP_006716618.1:p.Asn232=
XM_011517026.1:c.1043A=	XP_011515328.1:p.Asn348=
XM_005250914.3:c.158A=	XP_005250971.1:p.Asn53=
XM_006716555.3:c.695A=	XP_006716618.1:p.Asn232=
XM_011517026.2:c.1043A=	XP_011515328.1:p.Asn348=
XM_017013400.1:c.1181A=	XP_016868889.1:p.Asn394=
NM_004519.4:c.1403A= MANE Select	NP_004510.1:p.Asn468=
NM_001204824.2:c.1043A=	NP_001191753.1:p.Asn348=