Canonical Allele Identifier: CA1347589163

Gene: COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470423_15470426delinsTGGA , CM000665.2:g.15470423_15470426delinsTGGA	GRCh38
NC_000003.11:g.15511930_15511933delinsTGGA , CM000665.1:g.15511930_15511933delinsTGGA	GRCh37
NC_000003.10:g.15486934_15486937delinsTGGA	NCBI36
NG_009032.1:g.56326_56329delinsTCCA
NG_009032.2:g.56326_56329delinsTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.717+110_717+113delinsTCCA MANE Select	ENSP00000373298.3:n.717+110_717+113delinsTCCA
ENST00000604401.2:n.713+110_713+113delinsTCCA
ENST00000679838.1:c.*479+110_*479+113delinsTCCA	ENSP00000505708.1:n.*479+110_*479+113delinsTCCA
ENST00000680545.1:n.483+110_483+113delinsTCCA
ENST00000681097.1:c.717+110_717+113delinsTCCA	ENSP00000505397.1:n.717+110_717+113delinsTCCA
ENST00000383781.8:c.687+110_687+113delinsTCCA	ENSP00000373291.3:n.687+110_687+113delinsTCCA
ENST00000383786.9:c.615+110_615+113delinsTCCA	ENSP00000373296.3:n.615+110_615+113delinsTCCA
ENST00000383788.9:c.717+110_717+113delinsTCCA	ENSP00000373298.3:n.717+110_717+113delinsTCCA
ENST00000603808.5:c.717+110_717+113delinsTCCA	ENSP00000474271.1:n.717+110_717+113delinsTCCA
ENST00000605797.1:c.546+110_546+113delinsTCCA	ENSP00000474936.1:n.546+110_546+113delinsTCCA
NM_005677.3:c.717+110_717+113delinsTCCA	NP_005668.2:n.717+110_717+113delinsTCCA
NM_080538.2:c.687+110_687+113delinsTCCA	NP_536799.1:n.687+110_687+113delinsTCCA
NM_080539.3:c.615+110_615+113delinsTCCA	NP_536800.2:n.615+110_615+113delinsTCCA
NM_005677.4:c.717+110_717+113delinsTCCA MANE Select	NP_005668.2:n.717+110_717+113delinsTCCA
NM_080539.4:c.615+110_615+113delinsTCCA	NP_536800.2:n.615+110_615+113delinsTCCA