Canonical Allele Identifier: CA1347573710

Gene: EAF1-AS1 COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450883T= , CM000665.2:g.15450883T=	GRCh38
NC_000003.11:g.15492390T= , CM000665.1:g.15492390T=	GRCh37
NC_000003.10:g.15467394T=	NCBI36
NG_009032.1:g.75869A=
NG_009032.2:g.75869A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+562A= (EAF1-AS1)
ENST00000626521.1:n.55+562A= (EAF1-AS1)
ENST00000629729.3:c.414+562A=	ENSP00000518887.1:n.414+562A=
ENST00000383788.10:c.*761A= (COLQ) MANE Select	ENSP00000373298.3:n.*761A=
ENST00000679838.1:c.*1891A= (COLQ)	ENSP00000505708.1:n.*1891A=
ENST00000680545.1:n.1895A= (COLQ)
ENST00000680897.1:n.1594A= (COLQ)
ENST00000681097.1:c.*1143A= (COLQ)	ENSP00000505397.1:n.*1143A=
ENST00000681222.1:n.5620A= (COLQ)
ENST00000383781.8:c.*761A= (COLQ)	ENSP00000373291.3:n.*761A=
ENST00000383788.9:c.*761A= (COLQ)	ENSP00000373298.3:n.*761A=
NM_005677.3:c.*761A= (COLQ)	NP_005668.2:n.*761A=
NM_080538.2:c.*761A= (COLQ)	NP_536799.1:n.*761A=
NM_080539.3:c.*761A= (COLQ)	NP_536800.2:n.*761A=
NM_005677.4:c.*761A= (COLQ) MANE Select	NP_005668.2:n.*761A=
NM_080539.4:c.*761A= (COLQ)	NP_536800.2:n.*761A=