Canonical Allele Identifier: CA463070301

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133186552C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132174305C>G , CM000670.2:g.132174305C>G	GRCh38
NC_000008.10:g.133186552C>G , CM000670.1:g.133186552C>G	GRCh37
NC_000008.9:g.133255734C>G	NCBI36
NG_008854.2:g.311453G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000388996.10:c.978G>C MANE Select	ENSP00000373648.3:p.Thr326=
ENST00000521134.6:c.618G>C	ENSP00000429799.1:p.Thr206=
ENST00000638588.1:c.651G>C	ENSP00000491940.1:p.Thr217=
ENST00000639358.1:c.628G>C
ENST00000639496.1:c.651G>C	ENSP00000491165.1:p.Thr217=
ENST00000388996.8:c.978G>C	ENSP00000373648.3:p.Thr326=
ENST00000519445.5:c.978G>C	ENSP00000428790.1:p.Thr326=
ENST00000519589.1:n.756G>C
ENST00000521134.5:c.618G>C	ENSP00000429799.1:p.Thr206=
ENST00000621976.1:c.615G>C	ENSP00000482510.1:p.Thr205=
NM_001204824.1:c.618G>C	NP_001191753.1:p.Thr206=
NM_004519.3:c.978G>C	NP_004510.1:p.Thr326=
XM_005250914.2:c.-179G>C	XP_005250971.1:n.-179G>C
XM_006716555.2:c.270G>C	XP_006716618.1:p.Thr90=
XM_011517026.1:c.618G>C	XP_011515328.1:p.Thr206=
XM_005250914.3:c.-179G>C	XP_005250971.1:n.-179G>C
XM_006716555.3:c.270G>C	XP_006716618.1:p.Thr90=
XM_011517026.2:c.618G>C	XP_011515328.1:p.Thr206=
XM_017013400.1:c.756G>C	XP_016868889.1:p.Thr252=
NM_004519.4:c.978G>C MANE Select	NP_004510.1:p.Thr326=
NM_001204824.2:c.618G>C	NP_001191753.1:p.Thr206=