Canonical Allele Identifier: CA432645532

Gene: COLQ

Linked Data

• MyVariant Identifiers: chr3:g.15520508C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15479001C>G , CM000665.2:g.15479001C>G	GRCh38
NC_000003.11:g.15520508C>G , CM000665.1:g.15520508C>G	GRCh37
NC_000003.10:g.15495512C>G	NCBI36
NG_009032.1:g.47751G>C
NG_009032.2:g.47751G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.369G>C MANE Select	ENSP00000373298.3:p.Gly123=
ENST00000679838.1:c.*131G>C	ENSP00000505708.1:n.*131G>C
ENST00000681097.1:c.369G>C	ENSP00000505397.1:p.Gly123=
ENST00000383781.8:c.339G>C	ENSP00000373291.3:p.Gly113=
ENST00000383786.9:c.267G>C	ENSP00000373296.3:p.Gly89=
ENST00000383788.9:c.369G>C	ENSP00000373298.3:p.Gly123=
ENST00000603469.1:n.40G>C
ENST00000603808.5:c.369G>C	ENSP00000474271.1:p.Gly123=
ENST00000605797.1:c.198G>C	ENSP00000474936.1:p.Gly66=
NM_005677.3:c.369G>C	NP_005668.2:p.Gly123=
NM_080538.2:c.339G>C	NP_536799.1:p.Gly113=
NM_080539.3:c.267G>C	NP_536800.2:p.Gly89=
NM_005677.4:c.369G>C MANE Select	NP_005668.2:p.Gly123=
NM_080539.4:c.267G>C	NP_536800.2:p.Gly89=