Canonical Allele Identifier: CA1347573591

Gene: EAF1-AS1 COLQ EAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450576T= , CM000665.2:g.15450576T=	GRCh38
NC_000003.11:g.15492083T= , CM000665.1:g.15492083T=	GRCh37
NC_000003.10:g.15467087T=	NCBI36
NG_009032.1:g.76176A=
NG_009032.2:g.76176A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+869A= (EAF1-AS1)
ENST00000626521.1:n.55+869A= (EAF1-AS1)
ENST00000629729.3:c.414+869A=	ENSP00000518887.1:n.414+869A=
ENST00000383788.10:c.*1068A= (COLQ) MANE Select	ENSP00000373298.3:n.*1068A=
ENST00000679838.1:c.*2198A= (COLQ)	ENSP00000505708.1:n.*2198A=
ENST00000680545.1:n.2202A= (COLQ)
ENST00000680897.1:n.1901A= (COLQ)
ENST00000681097.1:c.*1450A= (COLQ)	ENSP00000505397.1:n.*1450A=
ENST00000681222.1:n.5927A= (COLQ)
ENST00000383781.8:c.*1068A= (COLQ)	ENSP00000373291.3:n.*1068A=
ENST00000383788.9:c.*1068A= (COLQ)	ENSP00000373298.3:n.*1068A=
ENST00000603752.1:n.304A= (COLQ)
ENST00000617675.1:n.497T= (EAF1)
NM_005677.3:c.*1068A= (COLQ)	NP_005668.2:n.*1068A=
NM_080538.2:c.*1068A= (COLQ)	NP_536799.1:n.*1068A=
NM_080539.3:c.*1068A= (COLQ)	NP_536800.2:n.*1068A=
NM_005677.4:c.*1068A= (COLQ) MANE Select	NP_005668.2:n.*1068A=
NM_080539.4:c.*1068A= (COLQ)	NP_536800.2:n.*1068A=