Canonical Allele Identifier: CA1820664553

Gene: KCNQ3

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175547T= , CM000670.2:g.132175547T=	GRCh38
NC_000008.10:g.133187794T= , CM000670.1:g.133187794T=	GRCh37
NC_000008.9:g.133256976T=	NCBI36
NG_008854.2:g.310211A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.839A= MANE Select	ENSP00000373648.3:p.Tyr280=
ENST00000521134.6:c.479A=	ENSP00000429799.1:p.Tyr160=
ENST00000638588.1:c.512A=	ENSP00000491940.1:p.Tyr171=
ENST00000639358.1:c.489A=
ENST00000639496.1:c.512A=	ENSP00000491165.1:p.Tyr171=
ENST00000388996.8:c.839A=	ENSP00000373648.3:p.Tyr280=
ENST00000519445.5:c.839A=	ENSP00000428790.1:p.Tyr280=
ENST00000519589.1:n.617A=
ENST00000521134.5:c.479A=	ENSP00000429799.1:p.Tyr160=
ENST00000621976.1:c.476A=	ENSP00000482510.1:p.Tyr159=
NM_001204824.1:c.479A=	NP_001191753.1:p.Tyr160=
NM_004519.3:c.839A=	NP_004510.1:p.Tyr280=
XM_005250914.2:c.-318A=	XP_005250971.1:n.-318A=
XM_006716555.2:c.131A=	XP_006716618.1:p.Tyr44=
XM_011517026.1:c.479A=	XP_011515328.1:p.Tyr160=
XM_005250914.3:c.-318A=	XP_005250971.1:n.-318A=
XM_006716555.3:c.131A=	XP_006716618.1:p.Tyr44=
XM_011517026.2:c.479A=	XP_011515328.1:p.Tyr160=
XM_017013400.1:c.617A=	XP_016868889.1:p.Tyr206=
NM_004519.4:c.839A= MANE Select	NP_004510.1:p.Tyr280=
NM_001204824.2:c.479A=	NP_001191753.1:p.Tyr160=