Canonical Allele Identifier: CA1820664386

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175161C= , CM000670.2:g.132175161C=	GRCh38
NC_000008.10:g.133187408C= , CM000670.1:g.133187408C=	GRCh37
NC_000008.9:g.133256590C=	NCBI36
NG_008854.2:g.310597G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.933+292G= MANE Select	ENSP00000373648.3:n.933+292G=
ENST00000521134.6:c.573+292G=	ENSP00000429799.1:n.573+292G=
ENST00000638588.1:c.606+292G=	ENSP00000491940.1:n.606+292G=
ENST00000639358.1:c.583+292G=
ENST00000639496.1:c.606+292G=	ENSP00000491165.1:n.606+292G=
ENST00000388996.8:c.933+292G=	ENSP00000373648.3:n.933+292G=
ENST00000519445.5:c.933+292G=	ENSP00000428790.1:n.933+292G=
ENST00000519589.1:n.711+292G=
ENST00000521134.5:c.573+292G=	ENSP00000429799.1:n.573+292G=
ENST00000621976.1:c.570+292G=	ENSP00000482510.1:n.570+292G=
NM_001204824.1:c.573+292G=	NP_001191753.1:n.573+292G=
NM_004519.3:c.933+292G=	NP_004510.1:n.933+292G=
XM_005250914.2:c.-224+292G=	XP_005250971.1:n.-224+292G=
XM_006716555.2:c.225+292G=	XP_006716618.1:n.225+292G=
XM_011517026.1:c.573+292G=	XP_011515328.1:n.573+292G=
XM_005250914.3:c.-224+292G=	XP_005250971.1:n.-224+292G=
XM_006716555.3:c.225+292G=	XP_006716618.1:n.225+292G=
XM_011517026.2:c.573+292G=	XP_011515328.1:n.573+292G=
XM_017013400.1:c.711+292G=	XP_016868889.1:n.711+292G=
NM_004519.4:c.933+292G= MANE Select	NP_004510.1:n.933+292G=
NM_001204824.2:c.573+292G=	NP_001191753.1:n.573+292G=