Canonical Allele Identifier: CA1347573630

Gene: EAF1-AS1 COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450683G= , CM000665.2:g.15450683G=	GRCh38
NC_000003.11:g.15492190G= , CM000665.1:g.15492190G=	GRCh37
NC_000003.10:g.15467194G=	NCBI36
NG_009032.1:g.76069C=
NG_009032.2:g.76069C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+762C= (EAF1-AS1)
ENST00000626521.1:n.55+762C= (EAF1-AS1)
ENST00000629729.3:c.414+762C=	ENSP00000518887.1:n.414+762C=
ENST00000383788.10:c.*961C= (COLQ) MANE Select	ENSP00000373298.3:n.*961C=
ENST00000679838.1:c.*2091C= (COLQ)	ENSP00000505708.1:n.*2091C=
ENST00000680545.1:n.2095C= (COLQ)
ENST00000680897.1:n.1794C= (COLQ)
ENST00000681097.1:c.*1343C= (COLQ)	ENSP00000505397.1:n.*1343C=
ENST00000681222.1:n.5820C= (COLQ)
ENST00000383781.8:c.*961C= (COLQ)	ENSP00000373291.3:n.*961C=
ENST00000383788.9:c.*961C= (COLQ)	ENSP00000373298.3:n.*961C=
ENST00000603752.1:n.197C= (COLQ)
NM_005677.3:c.*961C= (COLQ)	NP_005668.2:n.*961C=
NM_080538.2:c.*961C= (COLQ)	NP_536799.1:n.*961C=
NM_080539.3:c.*961C= (COLQ)	NP_536800.2:n.*961C=
NM_005677.4:c.*961C= (COLQ) MANE Select	NP_005668.2:n.*961C=
NM_080539.4:c.*961C= (COLQ)	NP_536800.2:n.*961C=