Canonical Allele Identifier: CA372290425

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133187759G>A (hg19) ; chr8:g.132175512G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175512G>A , CM000670.2:g.132175512G>A	GRCh38
NC_000008.10:g.133187759G>A , CM000670.1:g.133187759G>A	GRCh37
NC_000008.9:g.133256941G>A	NCBI36
NG_008854.2:g.310246C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.874C>T MANE Select	ENSP00000373648.3:p.Gln292Ter
ENST00000521134.6:c.514C>T	ENSP00000429799.1:p.Gln172Ter
ENST00000638588.1:c.547C>T	ENSP00000491940.1:p.Gln183Ter
ENST00000639358.1:c.524C>T
ENST00000639496.1:c.547C>T	ENSP00000491165.1:p.Gln183Ter
ENST00000388996.8:c.874C>T	ENSP00000373648.3:p.Gln292Ter
ENST00000519445.5:c.874C>T	ENSP00000428790.1:p.Gln292Ter
ENST00000519589.1:n.652C>T
ENST00000521134.5:c.514C>T	ENSP00000429799.1:p.Gln172Ter
ENST00000621976.1:c.511C>T	ENSP00000482510.1:p.Gln171Ter
NM_001204824.1:c.514C>T	NP_001191753.1:p.Gln172Ter
NM_004519.3:c.874C>T	NP_004510.1:p.Gln292Ter
XM_005250914.2:c.-283C>T	XP_005250971.1:n.-283C>T
XM_006716555.2:c.166C>T	XP_006716618.1:p.Gln56Ter
XM_011517026.1:c.514C>T	XP_011515328.1:p.Gln172Ter
XM_005250914.3:c.-283C>T	XP_005250971.1:n.-283C>T
XM_006716555.3:c.166C>T	XP_006716618.1:p.Gln56Ter
XM_011517026.2:c.514C>T	XP_011515328.1:p.Gln172Ter
XM_017013400.1:c.652C>T	XP_016868889.1:p.Gln218Ter
NM_004519.4:c.874C>T MANE Select	NP_004510.1:p.Gln292Ter
NM_001204824.2:c.514C>T	NP_001191753.1:p.Gln172Ter