Canonical Allele Identifier: CA2664638877

Gene: COLQ

Linked Data

• gnomAD v4: 3-15479286-ACAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15479287_15479289del , CM000665.2:g.15479287_15479289del	GRCh38
NC_000003.11:g.15520794_15520796del , CM000665.1:g.15520794_15520796del	GRCh37
NC_000003.10:g.15495798_15495800del	NCBI36
NG_009032.1:g.47463_47465del
NG_009032.2:g.47463_47465del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.366+49_366+51del MANE Select	ENSP00000373298.3:n.366+49_366+51del
ENST00000679838.1:c.*128+49_*128+51del	ENSP00000505708.1:n.*128+49_*128+51del
ENST00000681097.1:c.366+49_366+51del	ENSP00000505397.1:n.366+49_366+51del
ENST00000383781.8:c.336+49_336+51del	ENSP00000373291.3:n.336+49_336+51del
ENST00000383786.9:c.264+49_264+51del	ENSP00000373296.3:n.264+49_264+51del
ENST00000383788.9:c.366+49_366+51del	ENSP00000373298.3:n.366+49_366+51del
ENST00000603469.1:n.37+49_37+51del
ENST00000603808.5:c.366+49_366+51del	ENSP00000474271.1:n.366+49_366+51del
ENST00000605797.1:c.195+49_195+51del	ENSP00000474936.1:n.195+49_195+51del
NM_005677.3:c.366+49_366+51del	NP_005668.2:n.366+49_366+51del
NM_080538.2:c.336+49_336+51del	NP_536799.1:n.336+49_336+51del
NM_080539.3:c.264+49_264+51del	NP_536800.2:n.264+49_264+51del
NM_005677.4:c.366+49_366+51del MANE Select	NP_005668.2:n.366+49_366+51del
NM_080539.4:c.264+49_264+51del	NP_536800.2:n.264+49_264+51del