Canonical Allele Identifier: CA432645505

Gene: COLQ

Linked Data

• MyVariant Identifiers: chr3:g.15520490T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15478983T>G , CM000665.2:g.15478983T>G	GRCh38
NC_000003.11:g.15520490T>G , CM000665.1:g.15520490T>G	GRCh37
NC_000003.10:g.15495494T>G	NCBI36
NG_009032.1:g.47769A>C
NG_009032.2:g.47769A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000383788.10:c.387A>C MANE Select	ENSP00000373298.3:p.Gly129=
ENST00000679838.1:c.*149A>C	ENSP00000505708.1:n.*149A>C
ENST00000681097.1:c.387A>C	ENSP00000505397.1:p.Gly129=
ENST00000383781.8:c.357A>C	ENSP00000373291.3:p.Gly119=
ENST00000383786.9:c.285A>C	ENSP00000373296.3:p.Gly95=
ENST00000383788.9:c.387A>C	ENSP00000373298.3:p.Gly129=
ENST00000603469.1:n.58A>C
ENST00000603808.5:c.387A>C	ENSP00000474271.1:p.Gly129=
ENST00000605797.1:c.216A>C	ENSP00000474936.1:p.Gly72=
NM_005677.3:c.387A>C	NP_005668.2:p.Gly129=
NM_080538.2:c.357A>C	NP_536799.1:p.Gly119=
NM_080539.3:c.285A>C	NP_536800.2:p.Gly95=
NM_005677.4:c.387A>C MANE Select	NP_005668.2:p.Gly129=
NM_080539.4:c.285A>C	NP_536800.2:p.Gly95=