Canonical Allele Identifier: CA1820664519

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175469G= , CM000670.2:g.132175469G=	GRCh38
NC_000008.10:g.133187716G= , CM000670.1:g.133187716G=	GRCh37
NC_000008.9:g.133256898G=	NCBI36
NG_008854.2:g.310289C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.917C= MANE Select	ENSP00000373648.3:p.Ala306=
ENST00000521134.6:c.557C=	ENSP00000429799.1:p.Ala186=
ENST00000638588.1:c.590C=	ENSP00000491940.1:p.Ala197=
ENST00000639358.1:c.567C=
ENST00000639496.1:c.590C=	ENSP00000491165.1:p.Ala197=
ENST00000388996.8:c.917C=	ENSP00000373648.3:p.Ala306=
ENST00000519445.5:c.917C=	ENSP00000428790.1:p.Ala306=
ENST00000519589.1:n.695C=
ENST00000521134.5:c.557C=	ENSP00000429799.1:p.Ala186=
ENST00000621976.1:c.554C=	ENSP00000482510.1:p.Ala185=
NM_001204824.1:c.557C=	NP_001191753.1:p.Ala186=
NM_004519.3:c.917C=	NP_004510.1:p.Ala306=
XM_005250914.2:c.-240C=	XP_005250971.1:n.-240C=
XM_006716555.2:c.209C=	XP_006716618.1:p.Ala70=
XM_011517026.1:c.557C=	XP_011515328.1:p.Ala186=
XM_005250914.3:c.-240C=	XP_005250971.1:n.-240C=
XM_006716555.3:c.209C=	XP_006716618.1:p.Ala70=
XM_011517026.2:c.557C=	XP_011515328.1:p.Ala186=
XM_017013400.1:c.695C=	XP_016868889.1:p.Ala232=
NM_004519.4:c.917C= MANE Select	NP_004510.1:p.Ala306=
NM_001204824.2:c.557C=	NP_001191753.1:p.Ala186=