Canonical Allele Identifier: CA372290362

Gene: KCNQ3

Linked Data

• COSMIC: COSM5646950
• MyVariant Identifiers: chr8:g.133187733A>C (hg19) ; chr8:g.132175486A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175486A>C , CM000670.2:g.132175486A>C	GRCh38
NC_000008.10:g.133187733A>C , CM000670.1:g.133187733A>C	GRCh37
NC_000008.9:g.133256915A>C	NCBI36
NG_008854.2:g.310272T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000388996.10:c.900T>G MANE Select	ENSP00000373648.3:p.Phe300Leu
ENST00000521134.6:c.540T>G	ENSP00000429799.1:p.Phe180Leu
ENST00000638588.1:c.573T>G	ENSP00000491940.1:p.Phe191Leu
ENST00000639358.1:c.550T>G
ENST00000639496.1:c.573T>G	ENSP00000491165.1:p.Phe191Leu
ENST00000388996.8:c.900T>G	ENSP00000373648.3:p.Phe300Leu
ENST00000519445.5:c.900T>G	ENSP00000428790.1:p.Phe300Leu
ENST00000519589.1:n.678T>G
ENST00000521134.5:c.540T>G	ENSP00000429799.1:p.Phe180Leu
ENST00000621976.1:c.537T>G	ENSP00000482510.1:p.Phe179Leu
NM_001204824.1:c.540T>G	NP_001191753.1:p.Phe180Leu
NM_004519.3:c.900T>G	NP_004510.1:p.Phe300Leu
XM_005250914.2:c.-257T>G	XP_005250971.1:n.-257T>G
XM_006716555.2:c.192T>G	XP_006716618.1:p.Phe64Leu
XM_011517026.1:c.540T>G	XP_011515328.1:p.Phe180Leu
XM_005250914.3:c.-257T>G	XP_005250971.1:n.-257T>G
XM_006716555.3:c.192T>G	XP_006716618.1:p.Phe64Leu
XM_011517026.2:c.540T>G	XP_011515328.1:p.Phe180Leu
XM_017013400.1:c.678T>G	XP_016868889.1:p.Phe226Leu
NM_004519.4:c.900T>G MANE Select	NP_004510.1:p.Phe300Leu
NM_001204824.2:c.540T>G	NP_001191753.1:p.Phe180Leu