Canonical Allele Identifier: CA372290299

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133187705C>A (hg19) ; chr8:g.132175458C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175458C>A , CM000670.2:g.132175458C>A	GRCh38
NC_000008.10:g.133187705C>A , CM000670.1:g.133187705C>A	GRCh37
NC_000008.9:g.133256887C>A	NCBI36
NG_008854.2:g.310300G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.928G>T MANE Select	ENSP00000373648.3:p.Gly310Cys
ENST00000521134.6:c.568G>T	ENSP00000429799.1:p.Gly190Cys
ENST00000638588.1:c.601G>T	ENSP00000491940.1:p.Gly201Cys
ENST00000639358.1:c.578G>T
ENST00000639496.1:c.601G>T	ENSP00000491165.1:p.Gly201Cys
ENST00000388996.8:c.928G>T	ENSP00000373648.3:p.Gly310Cys
ENST00000519445.5:c.928G>T	ENSP00000428790.1:p.Gly310Cys
ENST00000519589.1:n.706G>T
ENST00000521134.5:c.568G>T	ENSP00000429799.1:p.Gly190Cys
ENST00000621976.1:c.565G>T	ENSP00000482510.1:p.Gly189Cys
NM_001204824.1:c.568G>T	NP_001191753.1:p.Gly190Cys
NM_004519.3:c.928G>T	NP_004510.1:p.Gly310Cys
XM_005250914.2:c.-229G>T	XP_005250971.1:n.-229G>T
XM_006716555.2:c.220G>T	XP_006716618.1:p.Gly74Cys
XM_011517026.1:c.568G>T	XP_011515328.1:p.Gly190Cys
XM_005250914.3:c.-229G>T	XP_005250971.1:n.-229G>T
XM_006716555.3:c.220G>T	XP_006716618.1:p.Gly74Cys
XM_011517026.2:c.568G>T	XP_011515328.1:p.Gly190Cys
XM_017013400.1:c.706G>T	XP_016868889.1:p.Gly236Cys
NM_004519.4:c.928G>T MANE Select	NP_004510.1:p.Gly310Cys
NM_001204824.2:c.568G>T	NP_001191753.1:p.Gly190Cys