Canonical Allele Identifier: CA1820664542

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175523T= , CM000670.2:g.132175523T=	GRCh38
NC_000008.10:g.133187770T= , CM000670.1:g.133187770T=	GRCh37
NC_000008.9:g.133256952T=	NCBI36
NG_008854.2:g.310235A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.863A= MANE Select	ENSP00000373648.3:p.Glu288=
ENST00000521134.6:c.503A=	ENSP00000429799.1:p.Glu168=
ENST00000638588.1:c.536A=	ENSP00000491940.1:p.Glu179=
ENST00000639358.1:c.513A=
ENST00000639496.1:c.536A=	ENSP00000491165.1:p.Glu179=
ENST00000388996.8:c.863A=	ENSP00000373648.3:p.Glu288=
ENST00000519445.5:c.863A=	ENSP00000428790.1:p.Glu288=
ENST00000519589.1:n.641A=
ENST00000521134.5:c.503A=	ENSP00000429799.1:p.Glu168=
ENST00000621976.1:c.500A=	ENSP00000482510.1:p.Glu167=
NM_001204824.1:c.503A=	NP_001191753.1:p.Glu168=
NM_004519.3:c.863A=	NP_004510.1:p.Glu288=
XM_005250914.2:c.-294A=	XP_005250971.1:n.-294A=
XM_006716555.2:c.155A=	XP_006716618.1:p.Glu52=
XM_011517026.1:c.503A=	XP_011515328.1:p.Glu168=
XM_005250914.3:c.-294A=	XP_005250971.1:n.-294A=
XM_006716555.3:c.155A=	XP_006716618.1:p.Glu52=
XM_011517026.2:c.503A=	XP_011515328.1:p.Glu168=
XM_017013400.1:c.641A=	XP_016868889.1:p.Glu214=
NM_004519.4:c.863A= MANE Select	NP_004510.1:p.Glu288=
NM_001204824.2:c.503A=	NP_001191753.1:p.Glu168=