Canonical Allele Identifier: CA1347587518

Gene: COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15466446G= , CM000665.2:g.15466446G=	GRCh38
NC_000003.11:g.15507953G= , CM000665.1:g.15507953G=	GRCh37
NC_000003.10:g.15482957G=	NCBI36
NG_009032.1:g.60306C=
NG_009032.2:g.60306C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000383788.10:c.718-9C= MANE Select	ENSP00000373298.3:n.718-9C=
ENST00000604401.2:n.714-9C=
ENST00000679838.1:c.*480-9C=	ENSP00000505708.1:n.*480-9C=
ENST00000680545.1:n.484-9C=
ENST00000681097.1:c.718-9C=	ENSP00000505397.1:n.718-9C=
ENST00000383781.8:c.688-9C=	ENSP00000373291.3:n.688-9C=
ENST00000383786.9:c.616-9C=	ENSP00000373296.3:n.616-9C=
ENST00000383788.9:c.718-9C=	ENSP00000373298.3:n.718-9C=
ENST00000603808.5:c.718-9C=	ENSP00000474271.1:n.718-9C=
ENST00000605797.1:c.547-9C=	ENSP00000474936.1:n.547-9C=
NM_005677.3:c.718-9C=	NP_005668.2:n.718-9C=
NM_080538.2:c.688-9C=	NP_536799.1:n.688-9C=
NM_080539.3:c.616-9C=	NP_536800.2:n.616-9C=
NM_005677.4:c.718-9C= MANE Select	NP_005668.2:n.718-9C=
NM_080539.4:c.616-9C=	NP_536800.2:n.616-9C=