Canonical Allele Identifier: CA372290626

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133187852G>C (hg19) ; chr8:g.132175605G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175605G>C , CM000670.2:g.132175605G>C	GRCh38
NC_000008.10:g.133187852G>C , CM000670.1:g.133187852G>C	GRCh37
NC_000008.9:g.133257034G>C	NCBI36
NG_008854.2:g.310153C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.781C>G MANE Select	ENSP00000373648.3:p.Leu261Val
ENST00000521134.6:c.421C>G	ENSP00000429799.1:p.Leu141Val
ENST00000638588.1:c.454C>G	ENSP00000491940.1:p.Leu152Val
ENST00000639358.1:c.431C>G
ENST00000639496.1:c.454C>G	ENSP00000491165.1:p.Leu152Val
ENST00000388996.8:c.781C>G	ENSP00000373648.3:p.Leu261Val
ENST00000519445.5:c.781C>G	ENSP00000428790.1:p.Leu261Val
ENST00000519589.1:n.559C>G
ENST00000521134.5:c.421C>G	ENSP00000429799.1:p.Leu141Val
ENST00000621976.1:c.418C>G	ENSP00000482510.1:p.Leu140Val
NM_001204824.1:c.421C>G	NP_001191753.1:p.Leu141Val
NM_004519.3:c.781C>G	NP_004510.1:p.Leu261Val
XM_005250914.2:c.-376C>G	XP_005250971.1:n.-376C>G
XM_006716555.2:c.73C>G	XP_006716618.1:p.Leu25Val
XM_011517026.1:c.421C>G	XP_011515328.1:p.Leu141Val
XM_005250914.3:c.-376C>G	XP_005250971.1:n.-376C>G
XM_006716555.3:c.73C>G	XP_006716618.1:p.Leu25Val
XM_011517026.2:c.421C>G	XP_011515328.1:p.Leu141Val
XM_017013400.1:c.559C>G	XP_016868889.1:p.Leu187Val
NM_004519.4:c.781C>G MANE Select	NP_004510.1:p.Leu261Val
NM_001204824.2:c.421C>G	NP_001191753.1:p.Leu141Val