Canonical Allele Identifier: CA1820664569

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175590A= , CM000670.2:g.132175590A=	GRCh38
NC_000008.10:g.133187837A= , CM000670.1:g.133187837A=	GRCh37
NC_000008.9:g.133257019A=	NCBI36
NG_008854.2:g.310168T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.796T= MANE Select	ENSP00000373648.3:p.Tyr266=
ENST00000521134.6:c.436T=	ENSP00000429799.1:p.Tyr146=
ENST00000638588.1:c.469T=	ENSP00000491940.1:p.Tyr157=
ENST00000639358.1:c.446T=
ENST00000639496.1:c.469T=	ENSP00000491165.1:p.Tyr157=
ENST00000388996.8:c.796T=	ENSP00000373648.3:p.Tyr266=
ENST00000519445.5:c.796T=	ENSP00000428790.1:p.Tyr266=
ENST00000519589.1:n.574T=
ENST00000521134.5:c.436T=	ENSP00000429799.1:p.Tyr146=
ENST00000621976.1:c.433T=	ENSP00000482510.1:p.Tyr145=
NM_001204824.1:c.436T=	NP_001191753.1:p.Tyr146=
NM_004519.3:c.796T=	NP_004510.1:p.Tyr266=
XM_005250914.2:c.-361T=	XP_005250971.1:n.-361T=
XM_006716555.2:c.88T=	XP_006716618.1:p.Tyr30=
XM_011517026.1:c.436T=	XP_011515328.1:p.Tyr146=
XM_005250914.3:c.-361T=	XP_005250971.1:n.-361T=
XM_006716555.3:c.88T=	XP_006716618.1:p.Tyr30=
XM_011517026.2:c.436T=	XP_011515328.1:p.Tyr146=
XM_017013400.1:c.574T=	XP_016868889.1:p.Tyr192=
NM_004519.4:c.796T= MANE Select	NP_004510.1:p.Tyr266=
NM_001204824.2:c.436T=	NP_001191753.1:p.Tyr146=