Canonical Allele Identifier: CA432643444

Gene: COLQ

Linked Data

• MyVariant Identifiers: chr3:g.15512085T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470578T>G , CM000665.2:g.15470578T>G	GRCh38
NC_000003.11:g.15512085T>G , CM000665.1:g.15512085T>G	GRCh37
NC_000003.10:g.15487089T>G	NCBI36
NG_009032.1:g.56174A>C
NG_009032.2:g.56174A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.675A>C MANE Select	ENSP00000373298.3:p.Gly225=
ENST00000604401.2:n.671A>C
ENST00000679838.1:c.*437A>C	ENSP00000505708.1:n.*437A>C
ENST00000680545.1:n.441A>C
ENST00000681097.1:c.675A>C	ENSP00000505397.1:p.Gly225=
ENST00000383781.8:c.645A>C	ENSP00000373291.3:p.Gly215=
ENST00000383786.9:c.573A>C	ENSP00000373296.3:p.Gly191=
ENST00000383788.9:c.675A>C	ENSP00000373298.3:p.Gly225=
ENST00000603808.5:c.675A>C	ENSP00000474271.1:p.Gly225=
ENST00000605797.1:c.504A>C	ENSP00000474936.1:p.Gly168=
NM_005677.3:c.675A>C	NP_005668.2:p.Gly225=
NM_080538.2:c.645A>C	NP_536799.1:p.Gly215=
NM_080539.3:c.573A>C	NP_536800.2:p.Gly191=
NM_005677.4:c.675A>C MANE Select	NP_005668.2:p.Gly225=
NM_080539.4:c.573A>C	NP_536800.2:p.Gly191=