Canonical Allele Identifier: CA351597608

Gene: COLQ

Linked Data

• MyVariant Identifiers: chr3:g.15507904T>G (hg19) ; chr3:g.15466397T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15466397T>G , CM000665.2:g.15466397T>G	GRCh38
NC_000003.11:g.15507904T>G , CM000665.1:g.15507904T>G	GRCh37
NC_000003.10:g.15482908T>G	NCBI36
NG_009032.1:g.60355A>C
NG_009032.2:g.60355A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.758A>C MANE Select	ENSP00000373298.3:p.Lys253Thr
ENST00000604401.2:n.754A>C
ENST00000679838.1:c.*520A>C	ENSP00000505708.1:n.*520A>C
ENST00000680545.1:n.524A>C
ENST00000681097.1:c.758A>C	ENSP00000505397.1:p.Lys253Thr
ENST00000383781.8:c.728A>C	ENSP00000373291.3:p.Lys243Thr
ENST00000383786.9:c.656A>C	ENSP00000373296.3:p.Lys219Thr
ENST00000383788.9:c.758A>C	ENSP00000373298.3:p.Lys253Thr
ENST00000603808.5:c.758A>C	ENSP00000474271.1:p.Lys253Thr
NM_005677.3:c.758A>C	NP_005668.2:p.Lys253Thr
NM_080538.2:c.728A>C	NP_536799.1:p.Lys243Thr
NM_080539.3:c.656A>C	NP_536800.2:p.Lys219Thr
NM_005677.4:c.758A>C MANE Select	NP_005668.2:p.Lys253Thr
NM_080539.4:c.656A>C	NP_536800.2:p.Lys219Thr