Canonical Allele Identifier: CA372290532

Gene: KCNQ3

Linked Data

• dbSNP Id: rs1826521379
• MyVariant Identifiers: chr8:g.133187809G>T (hg19) ; chr8:g.132175562G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175562G>T , CM000670.2:g.132175562G>T	GRCh38
NC_000008.10:g.133187809G>T , CM000670.1:g.133187809G>T	GRCh37
NC_000008.9:g.133256991G>T	NCBI36
NG_008854.2:g.310196C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.824C>A MANE Select	ENSP00000373648.3:p.Ser275Tyr
ENST00000521134.6:c.464C>A	ENSP00000429799.1:p.Ser155Tyr
ENST00000638588.1:c.497C>A	ENSP00000491940.1:p.Ser166Tyr
ENST00000639358.1:c.474C>A
ENST00000639496.1:c.497C>A	ENSP00000491165.1:p.Ser166Tyr
ENST00000388996.8:c.824C>A	ENSP00000373648.3:p.Ser275Tyr
ENST00000519445.5:c.824C>A	ENSP00000428790.1:p.Ser275Tyr
ENST00000519589.1:n.602C>A
ENST00000521134.5:c.464C>A	ENSP00000429799.1:p.Ser155Tyr
ENST00000621976.1:c.461C>A	ENSP00000482510.1:p.Ser154Tyr
NM_001204824.1:c.464C>A	NP_001191753.1:p.Ser155Tyr
NM_004519.3:c.824C>A	NP_004510.1:p.Ser275Tyr
XM_005250914.2:c.-333C>A	XP_005250971.1:n.-333C>A
XM_006716555.2:c.116C>A	XP_006716618.1:p.Ser39Tyr
XM_011517026.1:c.464C>A	XP_011515328.1:p.Ser155Tyr
XM_005250914.3:c.-333C>A	XP_005250971.1:n.-333C>A
XM_006716555.3:c.116C>A	XP_006716618.1:p.Ser39Tyr
XM_011517026.2:c.464C>A	XP_011515328.1:p.Ser155Tyr
XM_017013400.1:c.602C>A	XP_016868889.1:p.Ser201Tyr
NM_004519.4:c.824C>A MANE Select	NP_004510.1:p.Ser275Tyr
NM_001204824.2:c.464C>A	NP_001191753.1:p.Ser155Tyr