Canonical Allele Identifier: CA1820664015

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132174251A= , CM000670.2:g.132174251A=	GRCh38
NC_000008.10:g.133186498A= , CM000670.1:g.133186498A=	GRCh37
NC_000008.9:g.133255680A=	NCBI36
NG_008854.2:g.311507T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.1032T= MANE Select	ENSP00000373648.3:p.Phe344=
ENST00000521134.6:c.672T=	ENSP00000429799.1:p.Phe224=
ENST00000638588.1:c.705T=	ENSP00000491940.1:p.Phe235=
ENST00000639358.1:c.682T=
ENST00000639496.1:c.705T=	ENSP00000491165.1:p.Phe235=
ENST00000388996.8:c.1032T=	ENSP00000373648.3:p.Phe344=
ENST00000519445.5:c.1032T=	ENSP00000428790.1:p.Phe344=
ENST00000519589.1:n.810T=
ENST00000521134.5:c.672T=	ENSP00000429799.1:p.Phe224=
ENST00000621976.1:c.669T=	ENSP00000482510.1:p.Phe223=
NM_001204824.1:c.672T=	NP_001191753.1:p.Phe224=
NM_004519.3:c.1032T=	NP_004510.1:p.Phe344=
XM_005250914.2:c.-125T=	XP_005250971.1:n.-125T=
XM_006716555.2:c.324T=	XP_006716618.1:p.Phe108=
XM_011517026.1:c.672T=	XP_011515328.1:p.Phe224=
XM_005250914.3:c.-125T=	XP_005250971.1:n.-125T=
XM_006716555.3:c.324T=	XP_006716618.1:p.Phe108=
XM_011517026.2:c.672T=	XP_011515328.1:p.Phe224=
XM_017013400.1:c.810T=	XP_016868889.1:p.Phe270=
NM_004519.4:c.1032T= MANE Select	NP_004510.1:p.Phe344=
NM_001204824.2:c.672T=	NP_001191753.1:p.Phe224=