Canonical Allele Identifier: CA1820664572

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175595G= , CM000670.2:g.132175595G=	GRCh38
NC_000008.10:g.133187842G= , CM000670.1:g.133187842G=	GRCh37
NC_000008.9:g.133257024G=	NCBI36
NG_008854.2:g.310163C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.791C= MANE Select	ENSP00000373648.3:p.Ala264=
ENST00000521134.6:c.431C=	ENSP00000429799.1:p.Ala144=
ENST00000638588.1:c.464C=	ENSP00000491940.1:p.Ala155=
ENST00000639358.1:c.441C=
ENST00000639496.1:c.464C=	ENSP00000491165.1:p.Ala155=
ENST00000388996.8:c.791C=	ENSP00000373648.3:p.Ala264=
ENST00000519445.5:c.791C=	ENSP00000428790.1:p.Ala264=
ENST00000519589.1:n.569C=
ENST00000521134.5:c.431C=	ENSP00000429799.1:p.Ala144=
ENST00000621976.1:c.428C=	ENSP00000482510.1:p.Ala143=
NM_001204824.1:c.431C=	NP_001191753.1:p.Ala144=
NM_004519.3:c.791C=	NP_004510.1:p.Ala264=
XM_005250914.2:c.-366C=	XP_005250971.1:n.-366C=
XM_006716555.2:c.83C=	XP_006716618.1:p.Ala28=
XM_011517026.1:c.431C=	XP_011515328.1:p.Ala144=
XM_005250914.3:c.-366C=	XP_005250971.1:n.-366C=
XM_006716555.3:c.83C=	XP_006716618.1:p.Ala28=
XM_011517026.2:c.431C=	XP_011515328.1:p.Ala144=
XM_017013400.1:c.569C=	XP_016868889.1:p.Ala190=
NM_004519.4:c.791C= MANE Select	NP_004510.1:p.Ala264=
NM_001204824.2:c.431C=	NP_001191753.1:p.Ala144=