Canonical Allele Identifier: CA463070285

Gene: KCNQ3

Linked Data

• gnomAD v4: 8-132174284-G-T
• MyVariant Identifiers: chr8:g.133186531G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132174284G>T , CM000670.2:g.132174284G>T	GRCh38
NC_000008.10:g.133186531G>T , CM000670.1:g.133186531G>T	GRCh37
NC_000008.9:g.133255713G>T	NCBI36
NG_008854.2:g.311474C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.999C>A MANE Select	ENSP00000373648.3:p.Ala333=
ENST00000521134.6:c.639C>A	ENSP00000429799.1:p.Ala213=
ENST00000638588.1:c.672C>A	ENSP00000491940.1:p.Ala224=
ENST00000639358.1:c.649C>A
ENST00000639496.1:c.672C>A	ENSP00000491165.1:p.Ala224=
ENST00000388996.8:c.999C>A	ENSP00000373648.3:p.Ala333=
ENST00000519445.5:c.999C>A	ENSP00000428790.1:p.Ala333=
ENST00000519589.1:n.777C>A
ENST00000521134.5:c.639C>A	ENSP00000429799.1:p.Ala213=
ENST00000621976.1:c.636C>A	ENSP00000482510.1:p.Ala212=
NM_001204824.1:c.639C>A	NP_001191753.1:p.Ala213=
NM_004519.3:c.999C>A	NP_004510.1:p.Ala333=
XM_005250914.2:c.-158C>A	XP_005250971.1:n.-158C>A
XM_006716555.2:c.291C>A	XP_006716618.1:p.Ala97=
XM_011517026.1:c.639C>A	XP_011515328.1:p.Ala213=
XM_005250914.3:c.-158C>A	XP_005250971.1:n.-158C>A
XM_006716555.3:c.291C>A	XP_006716618.1:p.Ala97=
XM_011517026.2:c.639C>A	XP_011515328.1:p.Ala213=
XM_017013400.1:c.777C>A	XP_016868889.1:p.Ala259=
NM_004519.4:c.999C>A MANE Select	NP_004510.1:p.Ala333=
NM_001204824.2:c.639C>A	NP_001191753.1:p.Ala213=