Canonical Allele Identifier: CA315599

Gene: KCNQ3

Linked Data

• ClinVar Variation Id: 205966
• ClinVar RCV Id: RCV000187971 ; RCV001852468
• dbSNP Id: rs796052678
• MyVariant Identifiers: chr8:g.133187716G>A (hg19) ; chr8:g.132175469G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175469G>A , CM000670.2:g.132175469G>A	GRCh38
NC_000008.10:g.133187716G>A , CM000670.1:g.133187716G>A	GRCh37
NC_000008.9:g.133256898G>A	NCBI36
NG_008854.2:g.310289C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.917C>T MANE Select	ENSP00000373648.3:p.Ala306Val
ENST00000521134.6:c.557C>T	ENSP00000429799.1:p.Ala186Val
ENST00000638588.1:c.590C>T	ENSP00000491940.1:p.Ala197Val
ENST00000639358.1:c.567C>T
ENST00000639496.1:c.590C>T	ENSP00000491165.1:p.Ala197Val
ENST00000388996.8:c.917C>T	ENSP00000373648.3:p.Ala306Val
ENST00000519445.5:c.917C>T	ENSP00000428790.1:p.Ala306Val
ENST00000519589.1:n.695C>T
ENST00000521134.5:c.557C>T	ENSP00000429799.1:p.Ala186Val
ENST00000621976.1:c.554C>T	ENSP00000482510.1:p.Ala185Val
NM_001204824.1:c.557C>T	NP_001191753.1:p.Ala186Val
NM_004519.3:c.917C>T	NP_004510.1:p.Ala306Val
XM_005250914.2:c.-240C>T	XP_005250971.1:n.-240C>T
XM_006716555.2:c.209C>T	XP_006716618.1:p.Ala70Val
XM_011517026.1:c.557C>T	XP_011515328.1:p.Ala186Val
XM_005250914.3:c.-240C>T	XP_005250971.1:n.-240C>T
XM_006716555.3:c.209C>T	XP_006716618.1:p.Ala70Val
XM_011517026.2:c.557C>T	XP_011515328.1:p.Ala186Val
XM_017013400.1:c.695C>T	XP_016868889.1:p.Ala232Val
NM_004519.4:c.917C>T MANE Select	NP_004510.1:p.Ala306Val
NM_001204824.2:c.557C>T	NP_001191753.1:p.Ala186Val