Canonical Allele Identifier: CA1347589164
Gene: COLQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15470424_15470431delinsGGAGTCAA , CM000665.2:g.15470424_15470431delinsGGAGTCAA GRCh38
NC_000003.11:g.15511931_15511938delinsGGAGTCAA , CM000665.1:g.15511931_15511938delinsGGAGTCAA GRCh37
NC_000003.10:g.15486935_15486942delinsGGAGTCAA NCBI36
NG_009032.1:g.56321_56328delinsTTGACTCC
NG_009032.2:g.56321_56328delinsTTGACTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000383788.10:c.717+105_717+112delinsTTGACTCC MANE Select ENSP00000373298.3:n.717+105_717+112delinsTTGACTCC
ENST00000604401.2:n.713+105_713+112delinsTTGACTCC
ENST00000679838.1:c.*479+105_*479+112delinsTTGACTCC ENSP00000505708.1:n.*479+105_*479+112delinsTTGACTCC
ENST00000680545.1:n.483+105_483+112delinsTTGACTCC
ENST00000681097.1:c.717+105_717+112delinsTTGACTCC ENSP00000505397.1:n.717+105_717+112delinsTTGACTCC
ENST00000383781.8:c.687+105_687+112delinsTTGACTCC ENSP00000373291.3:n.687+105_687+112delinsTTGACTCC
ENST00000383786.9:c.615+105_615+112delinsTTGACTCC ENSP00000373296.3:n.615+105_615+112delinsTTGACTCC
ENST00000383788.9:c.717+105_717+112delinsTTGACTCC ENSP00000373298.3:n.717+105_717+112delinsTTGACTCC
ENST00000603808.5:c.717+105_717+112delinsTTGACTCC ENSP00000474271.1:n.717+105_717+112delinsTTGACTCC
ENST00000605797.1:c.546+105_546+112delinsTTGACTCC ENSP00000474936.1:n.546+105_546+112delinsTTGACTCC
NM_005677.3:c.717+105_717+112delinsTTGACTCC NP_005668.2:n.717+105_717+112delinsTTGACTCC
NM_080538.2:c.687+105_687+112delinsTTGACTCC NP_536799.1:n.687+105_687+112delinsTTGACTCC
NM_080539.3:c.615+105_615+112delinsTTGACTCC NP_536800.2:n.615+105_615+112delinsTTGACTCC
NM_005677.4:c.717+105_717+112delinsTTGACTCC MANE Select NP_005668.2:n.717+105_717+112delinsTTGACTCC
NM_080539.4:c.615+105_615+112delinsTTGACTCC NP_536800.2:n.615+105_615+112delinsTTGACTCC