Canonical Allele Identifier: CA1820664555

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175558T= , CM000670.2:g.132175558T=	GRCh38
NC_000008.10:g.133187805T= , CM000670.1:g.133187805T=	GRCh37
NC_000008.9:g.133256987T=	NCBI36
NG_008854.2:g.310200A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.828A= MANE Select	ENSP00000373648.3:p.Ser276=
ENST00000521134.6:c.468A=	ENSP00000429799.1:p.Ser156=
ENST00000638588.1:c.501A=	ENSP00000491940.1:p.Ser167=
ENST00000639358.1:c.478A=
ENST00000639496.1:c.501A=	ENSP00000491165.1:p.Ser167=
ENST00000388996.8:c.828A=	ENSP00000373648.3:p.Ser276=
ENST00000519445.5:c.828A=	ENSP00000428790.1:p.Ser276=
ENST00000519589.1:n.606A=
ENST00000521134.5:c.468A=	ENSP00000429799.1:p.Ser156=
ENST00000621976.1:c.465A=	ENSP00000482510.1:p.Ser155=
NM_001204824.1:c.468A=	NP_001191753.1:p.Ser156=
NM_004519.3:c.828A=	NP_004510.1:p.Ser276=
XM_005250914.2:c.-329A=	XP_005250971.1:n.-329A=
XM_006716555.2:c.120A=	XP_006716618.1:p.Ser40=
XM_011517026.1:c.468A=	XP_011515328.1:p.Ser156=
XM_005250914.3:c.-329A=	XP_005250971.1:n.-329A=
XM_006716555.3:c.120A=	XP_006716618.1:p.Ser40=
XM_011517026.2:c.468A=	XP_011515328.1:p.Ser156=
XM_017013400.1:c.606A=	XP_016868889.1:p.Ser202=
NM_004519.4:c.828A= MANE Select	NP_004510.1:p.Ser276=
NM_001204824.2:c.468A=	NP_001191753.1:p.Ser156=