Canonical Allele Identifier: CA372290297

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133187704C>G (hg19) ; chr8:g.132175457C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175457C>G , CM000670.2:g.132175457C>G	GRCh38
NC_000008.10:g.133187704C>G , CM000670.1:g.133187704C>G	GRCh37
NC_000008.9:g.133256886C>G	NCBI36
NG_008854.2:g.310301G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.929G>C MANE Select	ENSP00000373648.3:p.Gly310Ala
ENST00000521134.6:c.569G>C	ENSP00000429799.1:p.Gly190Ala
ENST00000638588.1:c.602G>C	ENSP00000491940.1:p.Gly201Ala
ENST00000639358.1:c.579G>C
ENST00000639496.1:c.602G>C	ENSP00000491165.1:p.Gly201Ala
ENST00000388996.8:c.929G>C	ENSP00000373648.3:p.Gly310Ala
ENST00000519445.5:c.929G>C	ENSP00000428790.1:p.Gly310Ala
ENST00000519589.1:n.707G>C
ENST00000521134.5:c.569G>C	ENSP00000429799.1:p.Gly190Ala
ENST00000621976.1:c.566G>C	ENSP00000482510.1:p.Gly189Ala
NM_001204824.1:c.569G>C	NP_001191753.1:p.Gly190Ala
NM_004519.3:c.929G>C	NP_004510.1:p.Gly310Ala
XM_005250914.2:c.-228G>C	XP_005250971.1:n.-228G>C
XM_006716555.2:c.221G>C	XP_006716618.1:p.Gly74Ala
XM_011517026.1:c.569G>C	XP_011515328.1:p.Gly190Ala
XM_005250914.3:c.-228G>C	XP_005250971.1:n.-228G>C
XM_006716555.3:c.221G>C	XP_006716618.1:p.Gly74Ala
XM_011517026.2:c.569G>C	XP_011515328.1:p.Gly190Ala
XM_017013400.1:c.707G>C	XP_016868889.1:p.Gly236Ala
NM_004519.4:c.929G>C MANE Select	NP_004510.1:p.Gly310Ala
NM_001204824.2:c.569G>C	NP_001191753.1:p.Gly190Ala