Canonical Allele Identifier: CA2664659758

Gene: EAF1-AS1 COLQ

Linked Data

• gnomAD v4: 3-15450747-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450748del , CM000665.2:g.15450748del	GRCh38
NC_000003.11:g.15492255del , CM000665.1:g.15492255del	GRCh37
NC_000003.10:g.15467259del	NCBI36
NG_009032.1:g.76004del
NG_009032.2:g.76004del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+697del (EAF1-AS1)
ENST00000626521.1:n.55+697del (EAF1-AS1)
ENST00000629729.3:c.414+697del	ENSP00000518887.1:n.414+697del
ENST00000383788.10:c.*896del (COLQ) MANE Select	ENSP00000373298.3:n.*896del
ENST00000679838.1:c.*2026del (COLQ)	ENSP00000505708.1:n.*2026del
ENST00000680545.1:n.2030del (COLQ)
ENST00000680897.1:n.1729del (COLQ)
ENST00000681097.1:c.*1278del (COLQ)	ENSP00000505397.1:n.*1278del
ENST00000681222.1:n.5755del (COLQ)
ENST00000383781.8:c.*896del (COLQ)	ENSP00000373291.3:n.*896del
ENST00000383788.9:c.*896del (COLQ)	ENSP00000373298.3:n.*896del
ENST00000603752.1:n.132del (COLQ)
NM_005677.3:c.*896del (COLQ)	NP_005668.2:n.*896del
NM_080538.2:c.*896del (COLQ)	NP_536799.1:n.*896del
NM_080539.3:c.*896del (COLQ)	NP_536800.2:n.*896del
NM_005677.4:c.*896del (COLQ) MANE Select	NP_005668.2:n.*896del
NM_080539.4:c.*896del (COLQ)	NP_536800.2:n.*896del