Canonical Allele Identifier: CA351597952

Gene: COLQ

Linked Data

• MyVariant Identifiers: chr3:g.15512064T>G (hg19) ; chr3:g.15470557T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470557T>G , CM000665.2:g.15470557T>G	GRCh38
NC_000003.11:g.15512064T>G , CM000665.1:g.15512064T>G	GRCh37
NC_000003.10:g.15487068T>G	NCBI36
NG_009032.1:g.56195A>C
NG_009032.2:g.56195A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.696A>C MANE Select	ENSP00000373298.3:p.Arg232Ser
ENST00000604401.2:n.692A>C
ENST00000679838.1:c.*458A>C	ENSP00000505708.1:n.*458A>C
ENST00000680545.1:n.462A>C
ENST00000681097.1:c.696A>C	ENSP00000505397.1:p.Arg232Ser
ENST00000383781.8:c.666A>C	ENSP00000373291.3:p.Arg222Ser
ENST00000383786.9:c.594A>C	ENSP00000373296.3:p.Arg198Ser
ENST00000383788.9:c.696A>C	ENSP00000373298.3:p.Arg232Ser
ENST00000603808.5:c.696A>C	ENSP00000474271.1:p.Arg232Ser
ENST00000605797.1:c.525A>C	ENSP00000474936.1:p.Arg175Ser
NM_005677.3:c.696A>C	NP_005668.2:p.Arg232Ser
NM_080538.2:c.666A>C	NP_536799.1:p.Arg222Ser
NM_080539.3:c.594A>C	NP_536800.2:p.Arg198Ser
NM_005677.4:c.696A>C MANE Select	NP_005668.2:p.Arg232Ser
NM_080539.4:c.594A>C	NP_536800.2:p.Arg198Ser