Canonical Allele Identifier: CA351597891
Gene: COLQ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.15470541T>A , CM000665.2:g.15470541T>A GRCh38
NC_000003.11:g.15512048T>A , CM000665.1:g.15512048T>A GRCh37
NC_000003.10:g.15487052T>A NCBI36
NG_009032.1:g.56211A>T
NG_009032.2:g.56211A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000383788.10:c.712A>T MANE Select ENSP00000373298.3:p.Lys238Ter
ENST00000604401.2:n.708A>T
ENST00000679838.1:c.*474A>T ENSP00000505708.1:n.*474A>T
ENST00000680545.1:n.478A>T
ENST00000681097.1:c.712A>T ENSP00000505397.1:p.Lys238Ter
ENST00000383781.8:c.682A>T ENSP00000373291.3:p.Lys228Ter
ENST00000383786.9:c.610A>T ENSP00000373296.3:p.Lys204Ter
ENST00000383788.9:c.712A>T ENSP00000373298.3:p.Lys238Ter
ENST00000603808.5:c.712A>T ENSP00000474271.1:p.Lys238Ter
ENST00000605797.1:c.541A>T ENSP00000474936.1:p.Lys181Ter
NM_005677.3:c.712A>T NP_005668.2:p.Lys238Ter
NM_080538.2:c.682A>T NP_536799.1:p.Lys228Ter
NM_080539.3:c.610A>T NP_536800.2:p.Lys204Ter
NM_005677.4:c.712A>T MANE Select NP_005668.2:p.Lys238Ter
NM_080539.4:c.610A>T NP_536800.2:p.Lys204Ter