Canonical Allele Identifier: CA1347593042
Gene: COLQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15479143_15479144delinsGA , CM000665.2:g.15479143_15479144delinsGA GRCh38
NC_000003.11:g.15520650_15520651delinsGA , CM000665.1:g.15520650_15520651delinsGA GRCh37
NC_000003.10:g.15495654_15495655delinsGA NCBI36
NG_009032.1:g.47608_47609delinsTC
NG_009032.2:g.47608_47609delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000383788.10:c.367-141_367-140delinsTC MANE Select ENSP00000373298.3:n.367-141_367-140delinsTC
ENST00000679838.1:c.*129-141_*129-140delinsTC ENSP00000505708.1:n.*129-141_*129-140delinsTC
ENST00000681097.1:c.367-141_367-140delinsTC ENSP00000505397.1:n.367-141_367-140delinsTC
ENST00000383781.8:c.337-141_337-140delinsTC ENSP00000373291.3:n.337-141_337-140delinsTC
ENST00000383786.9:c.265-141_265-140delinsTC ENSP00000373296.3:n.265-141_265-140delinsTC
ENST00000383788.9:c.367-141_367-140delinsTC ENSP00000373298.3:n.367-141_367-140delinsTC
ENST00000603469.1:n.38-141_38-140delinsTC
ENST00000603808.5:c.367-141_367-140delinsTC ENSP00000474271.1:n.367-141_367-140delinsTC
ENST00000605797.1:c.196-141_196-140delinsTC ENSP00000474936.1:n.196-141_196-140delinsTC
NM_005677.3:c.367-141_367-140delinsTC NP_005668.2:n.367-141_367-140delinsTC
NM_080538.2:c.337-141_337-140delinsTC NP_536799.1:n.337-141_337-140delinsTC
NM_080539.3:c.265-141_265-140delinsTC NP_536800.2:n.265-141_265-140delinsTC
NM_005677.4:c.367-141_367-140delinsTC MANE Select NP_005668.2:n.367-141_367-140delinsTC
NM_080539.4:c.265-141_265-140delinsTC NP_536800.2:n.265-141_265-140delinsTC