Canonical Allele Identifier: CA463070297

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133186543G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132174296G>C , CM000670.2:g.132174296G>C	GRCh38
NC_000008.10:g.133186543G>C , CM000670.1:g.133186543G>C	GRCh37
NC_000008.9:g.133255725G>C	NCBI36
NG_008854.2:g.311462C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000388996.10:c.987C>G MANE Select	ENSP00000373648.3:p.Gly329=
ENST00000521134.6:c.627C>G	ENSP00000429799.1:p.Gly209=
ENST00000638588.1:c.660C>G	ENSP00000491940.1:p.Gly220=
ENST00000639358.1:c.637C>G
ENST00000639496.1:c.660C>G	ENSP00000491165.1:p.Gly220=
ENST00000388996.8:c.987C>G	ENSP00000373648.3:p.Gly329=
ENST00000519445.5:c.987C>G	ENSP00000428790.1:p.Gly329=
ENST00000519589.1:n.765C>G
ENST00000521134.5:c.627C>G	ENSP00000429799.1:p.Gly209=
ENST00000621976.1:c.624C>G	ENSP00000482510.1:p.Gly208=
NM_001204824.1:c.627C>G	NP_001191753.1:p.Gly209=
NM_004519.3:c.987C>G	NP_004510.1:p.Gly329=
XM_005250914.2:c.-170C>G	XP_005250971.1:n.-170C>G
XM_006716555.2:c.279C>G	XP_006716618.1:p.Gly93=
XM_011517026.1:c.627C>G	XP_011515328.1:p.Gly209=
XM_005250914.3:c.-170C>G	XP_005250971.1:n.-170C>G
XM_006716555.3:c.279C>G	XP_006716618.1:p.Gly93=
XM_011517026.2:c.627C>G	XP_011515328.1:p.Gly209=
XM_017013400.1:c.765C>G	XP_016868889.1:p.Gly255=
NM_004519.4:c.987C>G MANE Select	NP_004510.1:p.Gly329=
NM_001204824.2:c.627C>G	NP_001191753.1:p.Gly209=