Canonical Allele Identifier: CA372290371

Gene: KCNQ3

Linked Data

• ClinVar Variation Id: 2683029
• ClinVar RCV Id: RCV003481896
• MyVariant Identifiers: chr8:g.133187737T>A (hg19) ; chr8:g.132175490T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175490T>A , CM000670.2:g.132175490T>A	GRCh38
NC_000008.10:g.133187737T>A , CM000670.1:g.133187737T>A	GRCh37
NC_000008.9:g.133256919T>A	NCBI36
NG_008854.2:g.310268A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.896A>T MANE Select	ENSP00000373648.3:p.Glu299Val
ENST00000521134.6:c.536A>T	ENSP00000429799.1:p.Glu179Val
ENST00000638588.1:c.569A>T	ENSP00000491940.1:p.Glu190Val
ENST00000639358.1:c.546A>T
ENST00000639496.1:c.569A>T	ENSP00000491165.1:p.Glu190Val
ENST00000388996.8:c.896A>T	ENSP00000373648.3:p.Glu299Val
ENST00000519445.5:c.896A>T	ENSP00000428790.1:p.Glu299Val
ENST00000519589.1:n.674A>T
ENST00000521134.5:c.536A>T	ENSP00000429799.1:p.Glu179Val
ENST00000621976.1:c.533A>T	ENSP00000482510.1:p.Glu178Val
NM_001204824.1:c.536A>T	NP_001191753.1:p.Glu179Val
NM_004519.3:c.896A>T	NP_004510.1:p.Glu299Val
XM_005250914.2:c.-261A>T	XP_005250971.1:n.-261A>T
XM_006716555.2:c.188A>T	XP_006716618.1:p.Glu63Val
XM_011517026.1:c.536A>T	XP_011515328.1:p.Glu179Val
XM_005250914.3:c.-261A>T	XP_005250971.1:n.-261A>T
XM_006716555.3:c.188A>T	XP_006716618.1:p.Glu63Val
XM_011517026.2:c.536A>T	XP_011515328.1:p.Glu179Val
XM_017013400.1:c.674A>T	XP_016868889.1:p.Glu225Val
NM_004519.4:c.896A>T MANE Select	NP_004510.1:p.Glu299Val
NM_001204824.2:c.536A>T	NP_001191753.1:p.Glu179Val