Canonical Allele Identifier: CA2664634619

Gene: COLQ

Linked Data

• gnomAD v4: 3-15470700-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470701del , CM000665.2:g.15470701del	GRCh38
NC_000003.11:g.15512208del , CM000665.1:g.15512208del	GRCh37
NC_000003.10:g.15487212del	NCBI36
NG_009032.1:g.56051del
NG_009032.2:g.56051del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.637-85del MANE Select	ENSP00000373298.3:n.637-85del
ENST00000604401.2:n.633-85del
ENST00000679838.1:c.*399-85del	ENSP00000505708.1:n.*399-85del
ENST00000680545.1:n.403-85del
ENST00000681097.1:c.637-85del	ENSP00000505397.1:n.637-85del
ENST00000383781.8:c.607-85del	ENSP00000373291.3:n.607-85del
ENST00000383786.9:c.535-85del	ENSP00000373296.3:n.535-85del
ENST00000383788.9:c.637-85del	ENSP00000373298.3:n.637-85del
ENST00000603808.5:c.637-85del	ENSP00000474271.1:n.637-85del
ENST00000605797.1:c.466-85del	ENSP00000474936.1:n.466-85del
NM_005677.3:c.637-85del	NP_005668.2:n.637-85del
NM_080538.2:c.607-85del	NP_536799.1:n.607-85del
NM_080539.3:c.535-85del	NP_536800.2:n.535-85del
NM_005677.4:c.637-85del MANE Select	NP_005668.2:n.637-85del
NM_080539.4:c.535-85del	NP_536800.2:n.535-85del