Canonical Allele Identifier: CA1347589265
Gene: COLQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15470621_15470624delinsAAAG , CM000665.2:g.15470621_15470624delinsAAAG GRCh38
NC_000003.11:g.15512128_15512131delinsAAAG , CM000665.1:g.15512128_15512131delinsAAAG GRCh37
NC_000003.10:g.15487132_15487135delinsAAAG NCBI36
NG_009032.1:g.56128_56131delinsCTTT
NG_009032.2:g.56128_56131delinsCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000383788.10:c.637-8_637-5delinsCTTT MANE Select ENSP00000373298.3:n.637-8_637-5delinsCTTT...
ENST00000604401.2:n.633-8_633-5delinsCTTT
ENST00000679838.1:c.*399-8_*399-5delinsCTTT ENSP00000505708.1:n.*399-8_*399-5delinsCT...
ENST00000680545.1:n.403-8_403-5delinsCTTT
ENST00000681097.1:c.637-8_637-5delinsCTTT ENSP00000505397.1:n.637-8_637-5delinsCTTT...
ENST00000383781.8:c.607-8_607-5delinsCTTT ENSP00000373291.3:n.607-8_607-5delinsCTTT...
ENST00000383786.9:c.535-8_535-5delinsCTTT ENSP00000373296.3:n.535-8_535-5delinsCTTT...
ENST00000383788.9:c.637-8_637-5delinsCTTT ENSP00000373298.3:n.637-8_637-5delinsCTTT...
ENST00000603808.5:c.637-8_637-5delinsCTTT ENSP00000474271.1:n.637-8_637-5delinsCTTT...
ENST00000605797.1:c.466-8_466-5delinsCTTT ENSP00000474936.1:n.466-8_466-5delinsCTTT...
NM_005677.3:c.637-8_637-5delinsCTTT NP_005668.2:n.637-8_637-5delinsCTTT
NM_080538.2:c.607-8_607-5delinsCTTT NP_536799.1:n.607-8_607-5delinsCTTT
NM_080539.3:c.535-8_535-5delinsCTTT NP_536800.2:n.535-8_535-5delinsCTTT
NM_005677.4:c.637-8_637-5delinsCTTT MANE Select NP_005668.2:n.637-8_637-5delinsCTTT
NM_080539.4:c.535-8_535-5delinsCTTT NP_536800.2:n.535-8_535-5delinsCTTT