Canonical Allele Identifier: CA351597955

Gene: COLQ

Linked Data

• MyVariant Identifiers: chr3:g.15512065C>G (hg19) ; chr3:g.15470558C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470558C>G , CM000665.2:g.15470558C>G	GRCh38
NC_000003.11:g.15512065C>G , CM000665.1:g.15512065C>G	GRCh37
NC_000003.10:g.15487069C>G	NCBI36
NG_009032.1:g.56194G>C
NG_009032.2:g.56194G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.695G>C MANE Select	ENSP00000373298.3:p.Arg232Thr
ENST00000604401.2:n.691G>C
ENST00000679838.1:c.*457G>C	ENSP00000505708.1:n.*457G>C
ENST00000680545.1:n.461G>C
ENST00000681097.1:c.695G>C	ENSP00000505397.1:p.Arg232Thr
ENST00000383781.8:c.665G>C	ENSP00000373291.3:p.Arg222Thr
ENST00000383786.9:c.593G>C	ENSP00000373296.3:p.Arg198Thr
ENST00000383788.9:c.695G>C	ENSP00000373298.3:p.Arg232Thr
ENST00000603808.5:c.695G>C	ENSP00000474271.1:p.Arg232Thr
ENST00000605797.1:c.524G>C	ENSP00000474936.1:p.Arg175Thr
NM_005677.3:c.695G>C	NP_005668.2:p.Arg232Thr
NM_080538.2:c.665G>C	NP_536799.1:p.Arg222Thr
NM_080539.3:c.593G>C	NP_536800.2:p.Arg198Thr
NM_005677.4:c.695G>C MANE Select	NP_005668.2:p.Arg232Thr
NM_080539.4:c.593G>C	NP_536800.2:p.Arg198Thr