Canonical Allele Identifier: CA372290065

Gene: KCNQ3

Linked Data

• MyVariant Identifiers: chr8:g.133186498A>C (hg19) ; chr8:g.132174251A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132174251A>C , CM000670.2:g.132174251A>C	GRCh38
NC_000008.10:g.133186498A>C , CM000670.1:g.133186498A>C	GRCh37
NC_000008.9:g.133255680A>C	NCBI36
NG_008854.2:g.311507T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388996.10:c.1032T>G MANE Select	ENSP00000373648.3:p.Phe344Leu
ENST00000521134.6:c.672T>G	ENSP00000429799.1:p.Phe224Leu
ENST00000638588.1:c.705T>G	ENSP00000491940.1:p.Phe235Leu
ENST00000639358.1:c.682T>G
ENST00000639496.1:c.705T>G	ENSP00000491165.1:p.Phe235Leu
ENST00000388996.8:c.1032T>G	ENSP00000373648.3:p.Phe344Leu
ENST00000519445.5:c.1032T>G	ENSP00000428790.1:p.Phe344Leu
ENST00000519589.1:n.810T>G
ENST00000521134.5:c.672T>G	ENSP00000429799.1:p.Phe224Leu
ENST00000621976.1:c.669T>G	ENSP00000482510.1:p.Phe223Leu
NM_001204824.1:c.672T>G	NP_001191753.1:p.Phe224Leu
NM_004519.3:c.1032T>G	NP_004510.1:p.Phe344Leu
XM_005250914.2:c.-125T>G	XP_005250971.1:n.-125T>G
XM_006716555.2:c.324T>G	XP_006716618.1:p.Phe108Leu
XM_011517026.1:c.672T>G	XP_011515328.1:p.Phe224Leu
XM_005250914.3:c.-125T>G	XP_005250971.1:n.-125T>G
XM_006716555.3:c.324T>G	XP_006716618.1:p.Phe108Leu
XM_011517026.2:c.672T>G	XP_011515328.1:p.Phe224Leu
XM_017013400.1:c.810T>G	XP_016868889.1:p.Phe270Leu
NM_004519.4:c.1032T>G MANE Select	NP_004510.1:p.Phe344Leu
NM_001204824.2:c.672T>G	NP_001191753.1:p.Phe224Leu