Canonical Allele Identifier: CA1045354117

Gene: EAF1-AS1 COLQ

Linked Data

• dbSNP Id: rs2061931625
• gnomAD v3: 3-15450850-A-G
• gnomAD v4: 3-15450850-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450850A>G , CM000665.2:g.15450850A>G	GRCh38
NC_000003.11:g.15492357A>G , CM000665.1:g.15492357A>G	GRCh37
NC_000003.10:g.15467361A>G	NCBI36
NG_009032.1:g.75902T>C
NG_009032.2:g.75902T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+595T>C (EAF1-AS1)
ENST00000626521.1:n.55+595T>C (EAF1-AS1)
ENST00000629729.3:c.414+595T>C	ENSP00000518887.1:n.414+595T>C
ENST00000383788.10:c.*794T>C (COLQ) MANE Select	ENSP00000373298.3:n.*794T>C
ENST00000679838.1:c.*1924T>C (COLQ)	ENSP00000505708.1:n.*1924T>C
ENST00000680545.1:n.1928T>C (COLQ)
ENST00000680897.1:n.1627T>C (COLQ)
ENST00000681097.1:c.*1176T>C (COLQ)	ENSP00000505397.1:n.*1176T>C
ENST00000681222.1:n.5653T>C (COLQ)
ENST00000383781.8:c.*794T>C (COLQ)	ENSP00000373291.3:n.*794T>C
ENST00000383788.9:c.*794T>C (COLQ)	ENSP00000373298.3:n.*794T>C
ENST00000603752.1:n.30T>C (COLQ)
NM_005677.3:c.*794T>C (COLQ)	NP_005668.2:n.*794T>C
NM_080538.2:c.*794T>C (COLQ)	NP_536799.1:n.*794T>C
NM_080539.3:c.*794T>C (COLQ)	NP_536800.2:n.*794T>C
NM_005677.4:c.*794T>C (COLQ) MANE Select	NP_005668.2:n.*794T>C
NM_080539.4:c.*794T>C (COLQ)	NP_536800.2:n.*794T>C