Canonical Allele Identifier: CA372290442

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133187767A>G (hg19) ; chr8:g.132175520A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175520A>G , CM000670.2:g.132175520A>G	GRCh38
NC_000008.10:g.133187767A>G , CM000670.1:g.133187767A>G	GRCh37
NC_000008.9:g.133256949A>G	NCBI36
NG_008854.2:g.310238T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.866T>C MANE Select	ENSP00000373648.3:p.Val289Ala
ENST00000521134.6:c.506T>C	ENSP00000429799.1:p.Val169Ala
ENST00000638588.1:c.539T>C	ENSP00000491940.1:p.Val180Ala
ENST00000639358.1:c.516T>C
ENST00000639496.1:c.539T>C	ENSP00000491165.1:p.Val180Ala
ENST00000388996.8:c.866T>C	ENSP00000373648.3:p.Val289Ala
ENST00000519445.5:c.866T>C	ENSP00000428790.1:p.Val289Ala
ENST00000519589.1:n.644T>C
ENST00000521134.5:c.506T>C	ENSP00000429799.1:p.Val169Ala
ENST00000621976.1:c.503T>C	ENSP00000482510.1:p.Val168Ala
NM_001204824.1:c.506T>C	NP_001191753.1:p.Val169Ala
NM_004519.3:c.866T>C	NP_004510.1:p.Val289Ala
XM_005250914.2:c.-291T>C	XP_005250971.1:n.-291T>C
XM_006716555.2:c.158T>C	XP_006716618.1:p.Val53Ala
XM_011517026.1:c.506T>C	XP_011515328.1:p.Val169Ala
XM_005250914.3:c.-291T>C	XP_005250971.1:n.-291T>C
XM_006716555.3:c.158T>C	XP_006716618.1:p.Val53Ala
XM_011517026.2:c.506T>C	XP_011515328.1:p.Val169Ala
XM_017013400.1:c.644T>C	XP_016868889.1:p.Val215Ala
NM_004519.4:c.866T>C MANE Select	NP_004510.1:p.Val289Ala
NM_001204824.2:c.506T>C	NP_001191753.1:p.Val169Ala