Canonical Allele Identifier: CA463070398

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133187796G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132175549G>T , CM000670.2:g.132175549G>T	GRCh38
NC_000008.10:g.133187796G>T , CM000670.1:g.133187796G>T	GRCh37
NC_000008.9:g.133256978G>T	NCBI36
NG_008854.2:g.310209C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.837C>A MANE Select	ENSP00000373648.3:p.Val279=
ENST00000521134.6:c.477C>A	ENSP00000429799.1:p.Val159=
ENST00000638588.1:c.510C>A	ENSP00000491940.1:p.Val170=
ENST00000639358.1:c.487C>A
ENST00000639496.1:c.510C>A	ENSP00000491165.1:p.Val170=
ENST00000388996.8:c.837C>A	ENSP00000373648.3:p.Val279=
ENST00000519445.5:c.837C>A	ENSP00000428790.1:p.Val279=
ENST00000519589.1:n.615C>A
ENST00000521134.5:c.477C>A	ENSP00000429799.1:p.Val159=
ENST00000621976.1:c.474C>A	ENSP00000482510.1:p.Val158=
NM_001204824.1:c.477C>A	NP_001191753.1:p.Val159=
NM_004519.3:c.837C>A	NP_004510.1:p.Val279=
XM_005250914.2:c.-320C>A	XP_005250971.1:n.-320C>A
XM_006716555.2:c.129C>A	XP_006716618.1:p.Val43=
XM_011517026.1:c.477C>A	XP_011515328.1:p.Val159=
XM_005250914.3:c.-320C>A	XP_005250971.1:n.-320C>A
XM_006716555.3:c.129C>A	XP_006716618.1:p.Val43=
XM_011517026.2:c.477C>A	XP_011515328.1:p.Val159=
XM_017013400.1:c.615C>A	XP_016868889.1:p.Val205=
NM_004519.4:c.837C>A MANE Select	NP_004510.1:p.Val279=
NM_001204824.2:c.477C>A	NP_001191753.1:p.Val159=