Canonical Allele Identifier: CA432643522

Gene: COLQ

Linked Data

• MyVariant Identifiers: chr3:g.15512121A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470614A>G , CM000665.2:g.15470614A>G	GRCh38
NC_000003.11:g.15512121A>G , CM000665.1:g.15512121A>G	GRCh37
NC_000003.10:g.15487125A>G	NCBI36
NG_009032.1:g.56138T>C
NG_009032.2:g.56138T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000383788.10:c.639T>C MANE Select	ENSP00000373298.3:p.Gly213=
ENST00000604401.2:n.635T>C
ENST00000679838.1:c.*401T>C	ENSP00000505708.1:n.*401T>C
ENST00000680545.1:n.405T>C
ENST00000681097.1:c.639T>C	ENSP00000505397.1:p.Gly213=
ENST00000383781.8:c.609T>C	ENSP00000373291.3:p.Gly203=
ENST00000383786.9:c.537T>C	ENSP00000373296.3:p.Gly179=
ENST00000383788.9:c.639T>C	ENSP00000373298.3:p.Gly213=
ENST00000603808.5:c.639T>C	ENSP00000474271.1:p.Gly213=
ENST00000605797.1:c.468T>C	ENSP00000474936.1:p.Gly156=
NM_005677.3:c.639T>C	NP_005668.2:p.Gly213=
NM_080538.2:c.609T>C	NP_536799.1:p.Gly203=
NM_080539.3:c.537T>C	NP_536800.2:p.Gly179=
NM_005677.4:c.639T>C MANE Select	NP_005668.2:p.Gly213=
NM_080539.4:c.537T>C	NP_536800.2:p.Gly179=