Canonical Allele Identifier: CA432643494

Gene: COLQ

Linked Data

• MyVariant Identifiers: chr3:g.15512100T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470593T>C , CM000665.2:g.15470593T>C	GRCh38
NC_000003.11:g.15512100T>C , CM000665.1:g.15512100T>C	GRCh37
NC_000003.10:g.15487104T>C	NCBI36
NG_009032.1:g.56159A>G
NG_009032.2:g.56159A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.660A>G MANE Select	ENSP00000373298.3:p.Glu220=
ENST00000604401.2:n.656A>G
ENST00000679838.1:c.*422A>G	ENSP00000505708.1:n.*422A>G
ENST00000680545.1:n.426A>G
ENST00000681097.1:c.660A>G	ENSP00000505397.1:p.Glu220=
ENST00000383781.8:c.630A>G	ENSP00000373291.3:p.Glu210=
ENST00000383786.9:c.558A>G	ENSP00000373296.3:p.Glu186=
ENST00000383788.9:c.660A>G	ENSP00000373298.3:p.Glu220=
ENST00000603808.5:c.660A>G	ENSP00000474271.1:p.Glu220=
ENST00000605797.1:c.489A>G	ENSP00000474936.1:p.Glu163=
NM_005677.3:c.660A>G	NP_005668.2:p.Glu220=
NM_080538.2:c.630A>G	NP_536799.1:p.Glu210=
NM_080539.3:c.558A>G	NP_536800.2:p.Glu186=
NM_005677.4:c.660A>G MANE Select	NP_005668.2:p.Glu220=
NM_080539.4:c.558A>G	NP_536800.2:p.Glu186=