Canonical Allele Identifier: CA2739822837

Gene: COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470642A>C , CM000665.2:g.15470642A>C	GRCh38
NC_000003.11:g.15512149A>C , CM000665.1:g.15512149A>C	GRCh37
NC_000003.10:g.15487153A>C	NCBI36
NG_009032.1:g.56110T>G
NG_009032.2:g.56110T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.637-26T>G MANE Select	ENSP00000373298.3:n.637-26T>G
ENST00000604401.2:n.633-26T>G
ENST00000679838.1:c.*399-26T>G	ENSP00000505708.1:n.*399-26T>G
ENST00000680545.1:n.403-26T>G
ENST00000681097.1:c.637-26T>G	ENSP00000505397.1:n.637-26T>G
ENST00000383781.8:c.607-26T>G	ENSP00000373291.3:n.607-26T>G
ENST00000383786.9:c.535-26T>G	ENSP00000373296.3:n.535-26T>G
ENST00000383788.9:c.637-26T>G	ENSP00000373298.3:n.637-26T>G
ENST00000603808.5:c.637-26T>G	ENSP00000474271.1:n.637-26T>G
ENST00000605797.1:c.466-26T>G	ENSP00000474936.1:n.466-26T>G
NM_005677.3:c.637-26T>G	NP_005668.2:n.637-26T>G
NM_080538.2:c.607-26T>G	NP_536799.1:n.607-26T>G
NM_080539.3:c.535-26T>G	NP_536800.2:n.535-26T>G
NM_005677.4:c.637-26T>G MANE Select	NP_005668.2:n.637-26T>G
NM_080539.4:c.535-26T>G	NP_536800.2:n.535-26T>G