Canonical Allele Identifier: CA2755334210

Gene: COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470395_15470396insA , CM000665.2:g.15470395_15470396insA	GRCh38
NC_000003.11:g.15511902_15511903insA , CM000665.1:g.15511902_15511903insA	GRCh37
NC_000003.10:g.15486906_15486907insA	NCBI36
NG_009032.1:g.56356_56357insT
NG_009032.2:g.56356_56357insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.717+140_717+141insT MANE Select	ENSP00000373298.3:n.717+140_717+141insT
ENST00000604401.2:n.713+140_713+141insT
ENST00000679838.1:c.*479+140_*479+141insT	ENSP00000505708.1:n.*479+140_*479+141insT
ENST00000680545.1:n.483+140_483+141insT
ENST00000681097.1:c.717+140_717+141insT	ENSP00000505397.1:n.717+140_717+141insT
ENST00000383781.8:c.687+140_687+141insT	ENSP00000373291.3:n.687+140_687+141insT
ENST00000383786.9:c.615+140_615+141insT	ENSP00000373296.3:n.615+140_615+141insT
ENST00000383788.9:c.717+140_717+141insT	ENSP00000373298.3:n.717+140_717+141insT
ENST00000603808.5:c.717+140_717+141insT	ENSP00000474271.1:n.717+140_717+141insT
ENST00000605797.1:c.546+140_546+141insT	ENSP00000474936.1:n.546+140_546+141insT
NM_005677.3:c.717+140_717+141insT	NP_005668.2:n.717+140_717+141insT
NM_080538.2:c.687+140_687+141insT	NP_536799.1:n.687+140_687+141insT
NM_080539.3:c.615+140_615+141insT	NP_536800.2:n.615+140_615+141insT
NM_005677.4:c.717+140_717+141insT MANE Select	NP_005668.2:n.717+140_717+141insT
NM_080539.4:c.615+140_615+141insT	NP_536800.2:n.615+140_615+141insT