Canonical Allele Identifier: CA1820664529

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175492C= , CM000670.2:g.132175492C=	GRCh38
NC_000008.10:g.133187739C= , CM000670.1:g.133187739C=	GRCh37
NC_000008.9:g.133256921C=	NCBI36
NG_008854.2:g.310266G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000388996.10:c.894G= MANE Select	ENSP00000373648.3:p.Glu298=
ENST00000521134.6:c.534G=	ENSP00000429799.1:p.Glu178=
ENST00000638588.1:c.567G=	ENSP00000491940.1:p.Glu189=
ENST00000639358.1:c.544G=
ENST00000639496.1:c.567G=	ENSP00000491165.1:p.Glu189=
ENST00000388996.8:c.894G=	ENSP00000373648.3:p.Glu298=
ENST00000519445.5:c.894G=	ENSP00000428790.1:p.Glu298=
ENST00000519589.1:n.672G=
ENST00000521134.5:c.534G=	ENSP00000429799.1:p.Glu178=
ENST00000621976.1:c.531G=	ENSP00000482510.1:p.Glu177=
NM_001204824.1:c.534G=	NP_001191753.1:p.Glu178=
NM_004519.3:c.894G=	NP_004510.1:p.Glu298=
XM_005250914.2:c.-263G=	XP_005250971.1:n.-263G=
XM_006716555.2:c.186G=	XP_006716618.1:p.Glu62=
XM_011517026.1:c.534G=	XP_011515328.1:p.Glu178=
XM_005250914.3:c.-263G=	XP_005250971.1:n.-263G=
XM_006716555.3:c.186G=	XP_006716618.1:p.Glu62=
XM_011517026.2:c.534G=	XP_011515328.1:p.Glu178=
XM_017013400.1:c.672G=	XP_016868889.1:p.Glu224=
NM_004519.4:c.894G= MANE Select	NP_004510.1:p.Glu298=
NM_001204824.2:c.534G=	NP_001191753.1:p.Glu178=