Canonical Allele Identifier: CA1347573649

Gene: EAF1-AS1 COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450718C= , CM000665.2:g.15450718C=	GRCh38
NC_000003.11:g.15492225C= , CM000665.1:g.15492225C=	GRCh37
NC_000003.10:g.15467229C=	NCBI36
NG_009032.1:g.76034G=
NG_009032.2:g.76034G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+727G= (EAF1-AS1)
ENST00000626521.1:n.55+727G= (EAF1-AS1)
ENST00000629729.3:c.414+727G=	ENSP00000518887.1:n.414+727G=
ENST00000383788.10:c.*926G= (COLQ) MANE Select	ENSP00000373298.3:n.*926G=
ENST00000679838.1:c.*2056G= (COLQ)	ENSP00000505708.1:n.*2056G=
ENST00000680545.1:n.2060G= (COLQ)
ENST00000680897.1:n.1759G= (COLQ)
ENST00000681097.1:c.*1308G= (COLQ)	ENSP00000505397.1:n.*1308G=
ENST00000681222.1:n.5785G= (COLQ)
ENST00000383781.8:c.*926G= (COLQ)	ENSP00000373291.3:n.*926G=
ENST00000383788.9:c.*926G= (COLQ)	ENSP00000373298.3:n.*926G=
ENST00000603752.1:n.162G= (COLQ)
NM_005677.3:c.*926G= (COLQ)	NP_005668.2:n.*926G=
NM_080538.2:c.*926G= (COLQ)	NP_536799.1:n.*926G=
NM_080539.3:c.*926G= (COLQ)	NP_536800.2:n.*926G=
NM_005677.4:c.*926G= (COLQ) MANE Select	NP_005668.2:n.*926G=
NM_080539.4:c.*926G= (COLQ)	NP_536800.2:n.*926G=