Canonical Allele Identifier: CA1347573611

Gene: EAF1-AS1 COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450642C= , CM000665.2:g.15450642C=	GRCh38
NC_000003.11:g.15492149C= , CM000665.1:g.15492149C=	GRCh37
NC_000003.10:g.15467153C=	NCBI36
NG_009032.1:g.76110G=
NG_009032.2:g.76110G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+803G= (EAF1-AS1)
ENST00000626521.1:n.55+803G= (EAF1-AS1)
ENST00000629729.3:c.414+803G=	ENSP00000518887.1:n.414+803G=
ENST00000383788.10:c.*1002G= (COLQ) MANE Select	ENSP00000373298.3:n.*1002G=
ENST00000679838.1:c.*2132G= (COLQ)	ENSP00000505708.1:n.*2132G=
ENST00000680545.1:n.2136G= (COLQ)
ENST00000680897.1:n.1835G= (COLQ)
ENST00000681097.1:c.*1384G= (COLQ)	ENSP00000505397.1:n.*1384G=
ENST00000681222.1:n.5861G= (COLQ)
ENST00000383781.8:c.*1002G= (COLQ)	ENSP00000373291.3:n.*1002G=
ENST00000383788.9:c.*1002G= (COLQ)	ENSP00000373298.3:n.*1002G=
ENST00000603752.1:n.238G= (COLQ)
NM_005677.3:c.*1002G= (COLQ)	NP_005668.2:n.*1002G=
NM_080538.2:c.*1002G= (COLQ)	NP_536799.1:n.*1002G=
NM_080539.3:c.*1002G= (COLQ)	NP_536800.2:n.*1002G=
NM_005677.4:c.*1002G= (COLQ) MANE Select	NP_005668.2:n.*1002G=
NM_080539.4:c.*1002G= (COLQ)	NP_536800.2:n.*1002G=