Canonical Allele Identifier: CA463070437

Gene: KCNQ3

Linked Data

• gnomAD v4: 8-132175600-G-A
• MyVariant Identifiers: chr8:g.133187847G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175600G>A , CM000670.2:g.132175600G>A	GRCh38
NC_000008.10:g.133187847G>A , CM000670.1:g.133187847G>A	GRCh37
NC_000008.9:g.133257029G>A	NCBI36
NG_008854.2:g.310158C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.786C>T MANE Select	ENSP00000373648.3:p.Ile262=
ENST00000521134.6:c.426C>T	ENSP00000429799.1:p.Ile142=
ENST00000638588.1:c.459C>T	ENSP00000491940.1:p.Ile153=
ENST00000639358.1:c.436C>T
ENST00000639496.1:c.459C>T	ENSP00000491165.1:p.Ile153=
ENST00000388996.8:c.786C>T	ENSP00000373648.3:p.Ile262=
ENST00000519445.5:c.786C>T	ENSP00000428790.1:p.Ile262=
ENST00000519589.1:n.564C>T
ENST00000521134.5:c.426C>T	ENSP00000429799.1:p.Ile142=
ENST00000621976.1:c.423C>T	ENSP00000482510.1:p.Ile141=
NM_001204824.1:c.426C>T	NP_001191753.1:p.Ile142=
NM_004519.3:c.786C>T	NP_004510.1:p.Ile262=
XM_005250914.2:c.-371C>T	XP_005250971.1:n.-371C>T
XM_006716555.2:c.78C>T	XP_006716618.1:p.Ile26=
XM_011517026.1:c.426C>T	XP_011515328.1:p.Ile142=
XM_005250914.3:c.-371C>T	XP_005250971.1:n.-371C>T
XM_006716555.3:c.78C>T	XP_006716618.1:p.Ile26=
XM_011517026.2:c.426C>T	XP_011515328.1:p.Ile142=
XM_017013400.1:c.564C>T	XP_016868889.1:p.Ile188=
NM_004519.4:c.786C>T MANE Select	NP_004510.1:p.Ile262=
NM_001204824.2:c.426C>T	NP_001191753.1:p.Ile142=