Canonical Allele Identifier: CA463070272

Gene: KCNQ3

Linked Data

• gnomAD v4: 8-132174266-A-G
• MyVariant Identifiers: chr8:g.133186513A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132174266A>G , CM000670.2:g.132174266A>G	GRCh38
NC_000008.10:g.133186513A>G , CM000670.1:g.133186513A>G	GRCh37
NC_000008.9:g.133255695A>G	NCBI36
NG_008854.2:g.311492T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.1017T>C MANE Select	ENSP00000373648.3:p.Ile339=
ENST00000521134.6:c.657T>C	ENSP00000429799.1:p.Ile219=
ENST00000638588.1:c.690T>C	ENSP00000491940.1:p.Ile230=
ENST00000639358.1:c.667T>C
ENST00000639496.1:c.690T>C	ENSP00000491165.1:p.Ile230=
ENST00000388996.8:c.1017T>C	ENSP00000373648.3:p.Ile339=
ENST00000519445.5:c.1017T>C	ENSP00000428790.1:p.Ile339=
ENST00000519589.1:n.795T>C
ENST00000521134.5:c.657T>C	ENSP00000429799.1:p.Ile219=
ENST00000621976.1:c.654T>C	ENSP00000482510.1:p.Ile218=
NM_001204824.1:c.657T>C	NP_001191753.1:p.Ile219=
NM_004519.3:c.1017T>C	NP_004510.1:p.Ile339=
XM_005250914.2:c.-140T>C	XP_005250971.1:n.-140T>C
XM_006716555.2:c.309T>C	XP_006716618.1:p.Ile103=
XM_011517026.1:c.657T>C	XP_011515328.1:p.Ile219=
XM_005250914.3:c.-140T>C	XP_005250971.1:n.-140T>C
XM_006716555.3:c.309T>C	XP_006716618.1:p.Ile103=
XM_011517026.2:c.657T>C	XP_011515328.1:p.Ile219=
XM_017013400.1:c.795T>C	XP_016868889.1:p.Ile265=
NM_004519.4:c.1017T>C MANE Select	NP_004510.1:p.Ile339=
NM_001204824.2:c.657T>C	NP_001191753.1:p.Ile219=