Canonical Allele Identifier: CA432643465

Gene: COLQ

Linked Data

• MyVariant Identifiers: chr3:g.15512091T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470584T>A , CM000665.2:g.15470584T>A	GRCh38
NC_000003.11:g.15512091T>A , CM000665.1:g.15512091T>A	GRCh37
NC_000003.10:g.15487095T>A	NCBI36
NG_009032.1:g.56168A>T
NG_009032.2:g.56168A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.669A>T MANE Select	ENSP00000373298.3:p.Ile223=
ENST00000604401.2:n.665A>T
ENST00000679838.1:c.*431A>T	ENSP00000505708.1:n.*431A>T
ENST00000680545.1:n.435A>T
ENST00000681097.1:c.669A>T	ENSP00000505397.1:p.Ile223=
ENST00000383781.8:c.639A>T	ENSP00000373291.3:p.Ile213=
ENST00000383786.9:c.567A>T	ENSP00000373296.3:p.Ile189=
ENST00000383788.9:c.669A>T	ENSP00000373298.3:p.Ile223=
ENST00000603808.5:c.669A>T	ENSP00000474271.1:p.Ile223=
ENST00000605797.1:c.498A>T	ENSP00000474936.1:p.Ile166=
NM_005677.3:c.669A>T	NP_005668.2:p.Ile223=
NM_080538.2:c.639A>T	NP_536799.1:p.Ile213=
NM_080539.3:c.567A>T	NP_536800.2:p.Ile189=
NM_005677.4:c.669A>T MANE Select	NP_005668.2:p.Ile223=
NM_080539.4:c.567A>T	NP_536800.2:p.Ile189=