Canonical Allele Identifier: CA1347573642

Gene: EAF1-AS1 COLQ

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450708_15450710delinsTAG , CM000665.2:g.15450708_15450710delinsTAG	GRCh38
NC_000003.11:g.15492215_15492217delinsTAG , CM000665.1:g.15492215_15492217delinsTAG	GRCh37
NC_000003.10:g.15467219_15467221delinsTAG	NCBI36
NG_009032.1:g.76042_76044delinsCTA
NG_009032.2:g.76042_76044delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+735_398+737delinsCTA (EAF1-AS1)
ENST00000626521.1:n.55+735_55+737delinsCTA (EAF1-AS1)
ENST00000629729.3:c.414+735_414+737delinsCTA	ENSP00000518887.1:n.414+735_414+737delinsCTA
ENST00000383788.10:c.*934_*936delinsCTA (COLQ) MANE Select	ENSP00000373298.3:n.*934_*936delinsCTA
ENST00000679838.1:c.*2064_*2066delinsCTA (COLQ)	ENSP00000505708.1:n.*2064_*2066delinsCTA
ENST00000680545.1:n.2068_2070delinsCTA (COLQ)
ENST00000680897.1:n.1767_1769delinsCTA (COLQ)
ENST00000681097.1:c.*1316_*1318delinsCTA (COLQ)	ENSP00000505397.1:n.*1316_*1318delinsCTA
ENST00000681222.1:n.5793_5795delinsCTA (COLQ)
ENST00000383781.8:c.*934_*936delinsCTA (COLQ)	ENSP00000373291.3:n.*934_*936delinsCTA
ENST00000383788.9:c.*934_*936delinsCTA (COLQ)	ENSP00000373298.3:n.*934_*936delinsCTA
ENST00000603752.1:n.170_172delinsCTA (COLQ)
NM_005677.3:c.*934_*936delinsCTA (COLQ)	NP_005668.2:n.*934_*936delinsCTA
NM_080538.2:c.*934_*936delinsCTA (COLQ)	NP_536799.1:n.*934_*936delinsCTA
NM_080539.3:c.*934_*936delinsCTA (COLQ)	NP_536800.2:n.*934_*936delinsCTA
NM_005677.4:c.*934_*936delinsCTA (COLQ) MANE Select	NP_005668.2:n.*934_*936delinsCTA
NM_080539.4:c.*934_*936delinsCTA (COLQ)	NP_536800.2:n.*934_*936delinsCTA