Canonical Allele Identifier: CA2664659634

Gene: EAF1-AS1 COLQ EAF1

Linked Data

• gnomAD v4: 3-15450591-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450591T>C , CM000665.2:g.15450591T>C	GRCh38
NC_000003.11:g.15492098T>C , CM000665.1:g.15492098T>C	GRCh37
NC_000003.10:g.15467102T>C	NCBI36
NG_009032.1:g.76161A>G
NG_009032.2:g.76161A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+854A>G (EAF1-AS1)
ENST00000626521.1:n.55+854A>G (EAF1-AS1)
ENST00000629729.3:c.414+854A>G	ENSP00000518887.1:n.414+854A>G
ENST00000383788.10:c.*1053A>G (COLQ) MANE Select	ENSP00000373298.3:n.*1053A>G
ENST00000679838.1:c.*2183A>G (COLQ)	ENSP00000505708.1:n.*2183A>G
ENST00000680545.1:n.2187A>G (COLQ)
ENST00000680897.1:n.1886A>G (COLQ)
ENST00000681097.1:c.*1435A>G (COLQ)	ENSP00000505397.1:n.*1435A>G
ENST00000681222.1:n.5912A>G (COLQ)
ENST00000383781.8:c.*1053A>G (COLQ)	ENSP00000373291.3:n.*1053A>G
ENST00000383788.9:c.*1053A>G (COLQ)	ENSP00000373298.3:n.*1053A>G
ENST00000603752.1:n.289A>G (COLQ)
ENST00000617675.1:n.512T>C (EAF1)
NM_005677.3:c.*1053A>G (COLQ)	NP_005668.2:n.*1053A>G
NM_080538.2:c.*1053A>G (COLQ)	NP_536799.1:n.*1053A>G
NM_080539.3:c.*1053A>G (COLQ)	NP_536800.2:n.*1053A>G
NM_005677.4:c.*1053A>G (COLQ) MANE Select	NP_005668.2:n.*1053A>G
NM_080539.4:c.*1053A>G (COLQ)	NP_536800.2:n.*1053A>G