Canonical Allele Identifier: CA2276042

Gene: COLQ

Linked Data

• dbSNP Id: rs766040052
• ExAC: 3:15512188 G / T
• gnomAD v4: 3-15470681-G-T
• MyVariant Identifiers: chr3:g.15512188G>T (hg19) ; chr3:g.15470681G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15470681G>T , CM000665.2:g.15470681G>T	GRCh38
NC_000003.11:g.15512188G>T , CM000665.1:g.15512188G>T	GRCh37
NC_000003.10:g.15487192G>T	NCBI36
NG_009032.1:g.56071C>A
NG_009032.2:g.56071C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383788.10:c.637-65C>A MANE Select	ENSP00000373298.3:n.637-65C>A
ENST00000604401.2:n.633-65C>A
ENST00000679838.1:c.*399-65C>A	ENSP00000505708.1:n.*399-65C>A
ENST00000680545.1:n.403-65C>A
ENST00000681097.1:c.637-65C>A	ENSP00000505397.1:n.637-65C>A
ENST00000383781.8:c.607-65C>A	ENSP00000373291.3:n.607-65C>A
ENST00000383786.9:c.535-65C>A	ENSP00000373296.3:n.535-65C>A
ENST00000383788.9:c.637-65C>A	ENSP00000373298.3:n.637-65C>A
ENST00000603808.5:c.637-65C>A	ENSP00000474271.1:n.637-65C>A
ENST00000605797.1:c.466-65C>A	ENSP00000474936.1:n.466-65C>A
NM_005677.3:c.637-65C>A	NP_005668.2:n.637-65C>A
NM_080538.2:c.607-65C>A	NP_536799.1:n.607-65C>A
NM_080539.3:c.535-65C>A	NP_536800.2:n.535-65C>A
NM_005677.4:c.637-65C>A MANE Select	NP_005668.2:n.637-65C>A
NM_080539.4:c.535-65C>A	NP_536800.2:n.535-65C>A