Canonical Allele Identifier: CA1347573676

Gene: EAF1-AS1 COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450788C= , CM000665.2:g.15450788C=	GRCh38
NC_000003.11:g.15492295C= , CM000665.1:g.15492295C=	GRCh37
NC_000003.10:g.15467299C=	NCBI36
NG_009032.1:g.75964G=
NG_009032.2:g.75964G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+657G= (EAF1-AS1)
ENST00000626521.1:n.55+657G= (EAF1-AS1)
ENST00000629729.3:c.414+657G=	ENSP00000518887.1:n.414+657G=
ENST00000383788.10:c.*856G= (COLQ) MANE Select	ENSP00000373298.3:n.*856G=
ENST00000679838.1:c.*1986G= (COLQ)	ENSP00000505708.1:n.*1986G=
ENST00000680545.1:n.1990G= (COLQ)
ENST00000680897.1:n.1689G= (COLQ)
ENST00000681097.1:c.*1238G= (COLQ)	ENSP00000505397.1:n.*1238G=
ENST00000681222.1:n.5715G= (COLQ)
ENST00000383781.8:c.*856G= (COLQ)	ENSP00000373291.3:n.*856G=
ENST00000383788.9:c.*856G= (COLQ)	ENSP00000373298.3:n.*856G=
ENST00000603752.1:n.92G= (COLQ)
NM_005677.3:c.*856G= (COLQ)	NP_005668.2:n.*856G=
NM_080538.2:c.*856G= (COLQ)	NP_536799.1:n.*856G=
NM_080539.3:c.*856G= (COLQ)	NP_536800.2:n.*856G=
NM_005677.4:c.*856G= (COLQ) MANE Select	NP_005668.2:n.*856G=
NM_080539.4:c.*856G= (COLQ)	NP_536800.2:n.*856G=