Canonical Allele Identifier: CA1045358606

Gene: COLQ

Linked Data

• gnomAD v3: 3-15470655-CATGTG-C
• gnomAD v4: 3-15470655-CATGTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470656_15470660del , CM000665.2:g.15470656_15470660del	GRCh38
NC_000003.11:g.15512163_15512167del , CM000665.1:g.15512163_15512167del	GRCh37
NC_000003.10:g.15487167_15487171del	NCBI36
NG_009032.1:g.56092_56096del
NG_009032.2:g.56092_56096del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.637-44_637-40del MANE Select	ENSP00000373298.3:n.637-44_637-40del
ENST00000604401.2:n.633-44_633-40del
ENST00000679838.1:c.*399-44_*399-40del	ENSP00000505708.1:n.*399-44_*399-40del
ENST00000680545.1:n.403-44_403-40del
ENST00000681097.1:c.637-44_637-40del	ENSP00000505397.1:n.637-44_637-40del
ENST00000383781.8:c.607-44_607-40del	ENSP00000373291.3:n.607-44_607-40del
ENST00000383786.9:c.535-44_535-40del	ENSP00000373296.3:n.535-44_535-40del
ENST00000383788.9:c.637-44_637-40del	ENSP00000373298.3:n.637-44_637-40del
ENST00000603808.5:c.637-44_637-40del	ENSP00000474271.1:n.637-44_637-40del
ENST00000605797.1:c.466-44_466-40del	ENSP00000474936.1:n.466-44_466-40del
NM_005677.3:c.637-44_637-40del	NP_005668.2:n.637-44_637-40del
NM_080538.2:c.607-44_607-40del	NP_536799.1:n.607-44_607-40del
NM_080539.3:c.535-44_535-40del	NP_536800.2:n.535-44_535-40del
NM_005677.4:c.637-44_637-40del MANE Select	NP_005668.2:n.637-44_637-40del
NM_080539.4:c.535-44_535-40del	NP_536800.2:n.535-44_535-40del