Canonical Allele Identifier: CA372290468

Gene: KCNQ3

Linked Data

• gnomAD v4: 8-132175533-C-G
• MyVariant Identifiers: chr8:g.133187780C>G (hg19) ; chr8:g.132175533C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175533C>G , CM000670.2:g.132175533C>G	GRCh38
NC_000008.10:g.133187780C>G , CM000670.1:g.133187780C>G	GRCh37
NC_000008.9:g.133256962C>G	NCBI36
NG_008854.2:g.310225G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.853G>C MANE Select	ENSP00000373648.3:p.Asp285His
ENST00000521134.6:c.493G>C	ENSP00000429799.1:p.Asp165His
ENST00000638588.1:c.526G>C	ENSP00000491940.1:p.Asp176His
ENST00000639358.1:c.503G>C
ENST00000639496.1:c.526G>C	ENSP00000491165.1:p.Asp176His
ENST00000388996.8:c.853G>C	ENSP00000373648.3:p.Asp285His
ENST00000519445.5:c.853G>C	ENSP00000428790.1:p.Asp285His
ENST00000519589.1:n.631G>C
ENST00000521134.5:c.493G>C	ENSP00000429799.1:p.Asp165His
ENST00000621976.1:c.490G>C	ENSP00000482510.1:p.Asp164His
NM_001204824.1:c.493G>C	NP_001191753.1:p.Asp165His
NM_004519.3:c.853G>C	NP_004510.1:p.Asp285His
XM_005250914.2:c.-304G>C	XP_005250971.1:n.-304G>C
XM_006716555.2:c.145G>C	XP_006716618.1:p.Asp49His
XM_011517026.1:c.493G>C	XP_011515328.1:p.Asp165His
XM_005250914.3:c.-304G>C	XP_005250971.1:n.-304G>C
XM_006716555.3:c.145G>C	XP_006716618.1:p.Asp49His
XM_011517026.2:c.493G>C	XP_011515328.1:p.Asp165His
XM_017013400.1:c.631G>C	XP_016868889.1:p.Asp211His
NM_004519.4:c.853G>C MANE Select	NP_004510.1:p.Asp285His
NM_001204824.2:c.493G>C	NP_001191753.1:p.Asp165His