Canonical Allele Identifier: CA432645499

Gene: COLQ

Linked Data

• gnomAD v4: 3-15478980-C-T
• MyVariant Identifiers: chr3:g.15520487C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15478980C>T , CM000665.2:g.15478980C>T	GRCh38
NC_000003.11:g.15520487C>T , CM000665.1:g.15520487C>T	GRCh37
NC_000003.10:g.15495491C>T	NCBI36
NG_009032.1:g.47772G>A
NG_009032.2:g.47772G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000383788.10:c.390G>A MANE Select	ENSP00000373298.3:p.Arg130=
ENST00000679838.1:c.*152G>A	ENSP00000505708.1:n.*152G>A
ENST00000681097.1:c.390G>A	ENSP00000505397.1:p.Arg130=
ENST00000383781.8:c.360G>A	ENSP00000373291.3:p.Arg120=
ENST00000383786.9:c.288G>A	ENSP00000373296.3:p.Arg96=
ENST00000383788.9:c.390G>A	ENSP00000373298.3:p.Arg130=
ENST00000603469.1:n.61G>A
ENST00000603808.5:c.390G>A	ENSP00000474271.1:p.Arg130=
ENST00000605797.1:c.219G>A	ENSP00000474936.1:p.Arg73=
NM_005677.3:c.390G>A	NP_005668.2:p.Arg130=
NM_080538.2:c.360G>A	NP_536799.1:p.Arg120=
NM_080539.3:c.288G>A	NP_536800.2:p.Arg96=
NM_005677.4:c.390G>A MANE Select	NP_005668.2:p.Arg130=
NM_080539.4:c.288G>A	NP_536800.2:p.Arg96=