Canonical Allele Identifier: CA1820664575

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175599T= , CM000670.2:g.132175599T=	GRCh38
NC_000008.10:g.133187846T= , CM000670.1:g.133187846T=	GRCh37
NC_000008.9:g.133257028T=	NCBI36
NG_008854.2:g.310159A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.787A= MANE Select	ENSP00000373648.3:p.Thr263=
ENST00000521134.6:c.427A=	ENSP00000429799.1:p.Thr143=
ENST00000638588.1:c.460A=	ENSP00000491940.1:p.Thr154=
ENST00000639358.1:c.437A=
ENST00000639496.1:c.460A=	ENSP00000491165.1:p.Thr154=
ENST00000388996.8:c.787A=	ENSP00000373648.3:p.Thr263=
ENST00000519445.5:c.787A=	ENSP00000428790.1:p.Thr263=
ENST00000519589.1:n.565A=
ENST00000521134.5:c.427A=	ENSP00000429799.1:p.Thr143=
ENST00000621976.1:c.424A=	ENSP00000482510.1:p.Thr142=
NM_001204824.1:c.427A=	NP_001191753.1:p.Thr143=
NM_004519.3:c.787A=	NP_004510.1:p.Thr263=
XM_005250914.2:c.-370A=	XP_005250971.1:n.-370A=
XM_006716555.2:c.79A=	XP_006716618.1:p.Thr27=
XM_011517026.1:c.427A=	XP_011515328.1:p.Thr143=
XM_005250914.3:c.-370A=	XP_005250971.1:n.-370A=
XM_006716555.3:c.79A=	XP_006716618.1:p.Thr27=
XM_011517026.2:c.427A=	XP_011515328.1:p.Thr143=
XM_017013400.1:c.565A=	XP_016868889.1:p.Thr189=
NM_004519.4:c.787A= MANE Select	NP_004510.1:p.Thr263=
NM_001204824.2:c.427A=	NP_001191753.1:p.Thr143=