Canonical Allele Identifier: CA1820664568

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175589T= , CM000670.2:g.132175589T=	GRCh38
NC_000008.10:g.133187836T= , CM000670.1:g.133187836T=	GRCh37
NC_000008.9:g.133257018T=	NCBI36
NG_008854.2:g.310169A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.797A= MANE Select	ENSP00000373648.3:p.Tyr266=
ENST00000521134.6:c.437A=	ENSP00000429799.1:p.Tyr146=
ENST00000638588.1:c.470A=	ENSP00000491940.1:p.Tyr157=
ENST00000639358.1:c.447A=
ENST00000639496.1:c.470A=	ENSP00000491165.1:p.Tyr157=
ENST00000388996.8:c.797A=	ENSP00000373648.3:p.Tyr266=
ENST00000519445.5:c.797A=	ENSP00000428790.1:p.Tyr266=
ENST00000519589.1:n.575A=
ENST00000521134.5:c.437A=	ENSP00000429799.1:p.Tyr146=
ENST00000621976.1:c.434A=	ENSP00000482510.1:p.Tyr145=
NM_001204824.1:c.437A=	NP_001191753.1:p.Tyr146=
NM_004519.3:c.797A=	NP_004510.1:p.Tyr266=
XM_005250914.2:c.-360A=	XP_005250971.1:n.-360A=
XM_006716555.2:c.89A=	XP_006716618.1:p.Tyr30=
XM_011517026.1:c.437A=	XP_011515328.1:p.Tyr146=
XM_005250914.3:c.-360A=	XP_005250971.1:n.-360A=
XM_006716555.3:c.89A=	XP_006716618.1:p.Tyr30=
XM_011517026.2:c.437A=	XP_011515328.1:p.Tyr146=
XM_017013400.1:c.575A=	XP_016868889.1:p.Tyr192=
NM_004519.4:c.797A= MANE Select	NP_004510.1:p.Tyr266=
NM_001204824.2:c.437A=	NP_001191753.1:p.Tyr146=