Canonical Allele Identifier: CA1820651619

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132129419T= , CM000670.2:g.132129419T=	GRCh38
NC_000008.10:g.133141666T= , CM000670.1:g.133141666T=	GRCh37
NC_000008.9:g.133210848T=	NCBI36
NG_008854.2:g.356339A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.2462A= MANE Select	ENSP00000373648.3:p.Asn821=
ENST00000521134.6:c.2102A=	ENSP00000429799.1:p.Asn701=
ENST00000638588.1:c.2135A=	ENSP00000491940.1:p.Asn712=
ENST00000639496.1:c.*1086A=	ENSP00000491165.1:n.*1086A=
ENST00000388996.8:c.2462A=	ENSP00000373648.3:p.Asn821=
ENST00000519445.5:c.2426A=	ENSP00000428790.1:p.Asn809=
ENST00000519589.1:n.3190A=
ENST00000521134.5:c.2102A=	ENSP00000429799.1:p.Asn701=
ENST00000621976.1:c.2099A=	ENSP00000482510.1:p.Asn700=
NM_001204824.1:c.2102A=	NP_001191753.1:p.Asn701=
NM_004519.3:c.2462A=	NP_004510.1:p.Asn821=
XM_005250914.2:c.1217A=	XP_005250971.1:p.Asn406=
XM_006716555.2:c.1754A=	XP_006716618.1:p.Asn585=
XM_011517026.1:c.2102A=	XP_011515328.1:p.Asn701=
XM_005250914.3:c.1217A=	XP_005250971.1:p.Asn406=
XM_006716555.3:c.1754A=	XP_006716618.1:p.Asn585=
XM_011517026.2:c.2102A=	XP_011515328.1:p.Asn701=
XM_017013400.1:c.2240A=	XP_016868889.1:p.Asn747=
NM_004519.4:c.2462A= MANE Select	NP_004510.1:p.Asn821=
NM_001204824.2:c.2102A=	NP_001191753.1:p.Asn701=