Canonical Allele Identifier: CA351597503

Gene: COLQ

Linked Data

• dbSNP Id: rs1251683000
• gnomAD v2: 3-15507848-C-T
• gnomAD v4: 3-15466341-C-T
• MyVariant Identifiers: chr3:g.15507848C>T (hg19) ; chr3:g.15466341C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15466341C>T , CM000665.2:g.15466341C>T	GRCh38
NC_000003.11:g.15507848C>T , CM000665.1:g.15507848C>T	GRCh37
NC_000003.10:g.15482852C>T	NCBI36
NG_009032.1:g.60411G>A
NG_009032.2:g.60411G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000383788.10:c.814G>A MANE Select	ENSP00000373298.3:p.Gly272Arg
ENST00000604401.2:n.810G>A
ENST00000679838.1:c.*576G>A	ENSP00000505708.1:n.*576G>A
ENST00000680545.1:n.580G>A
ENST00000681097.1:c.814G>A	ENSP00000505397.1:p.Asp272Asn
ENST00000383781.8:c.784G>A	ENSP00000373291.3:p.Gly262Arg
ENST00000383786.9:c.712G>A	ENSP00000373296.3:p.Gly238Arg
ENST00000383788.9:c.814G>A	ENSP00000373298.3:p.Gly272Arg
ENST00000603808.5:c.814G>A	ENSP00000474271.1:p.Gly272Arg
NM_005677.3:c.814G>A	NP_005668.2:p.Gly272Arg
NM_080538.2:c.784G>A	NP_536799.1:p.Gly262Arg
NM_080539.3:c.712G>A	NP_536800.2:p.Gly238Arg
NM_005677.4:c.814G>A MANE Select	NP_005668.2:p.Gly272Arg
NM_080539.4:c.712G>A	NP_536800.2:p.Gly238Arg