Canonical Allele Identifier: CA2592960022

Gene: EAF1-AS1 COLQ

Linked Data

• gnomAD v3: 3-15450891-G-A
• gnomAD v4: 3-15450891-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450891G>A , CM000665.2:g.15450891G>A	GRCh38
NC_000003.11:g.15492398G>A , CM000665.1:g.15492398G>A	GRCh37
NC_000003.10:g.15467402G>A	NCBI36
NG_009032.1:g.75861C>T
NG_009032.2:g.75861C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+554C>T (EAF1-AS1)
ENST00000626521.1:n.55+554C>T (EAF1-AS1)
ENST00000629729.3:c.414+554C>T	ENSP00000518887.1:n.414+554C>T
ENST00000383788.10:c.*753C>T (COLQ) MANE Select	ENSP00000373298.3:n.*753C>T
ENST00000679838.1:c.*1883C>T (COLQ)	ENSP00000505708.1:n.*1883C>T
ENST00000680545.1:n.1887C>T (COLQ)
ENST00000680897.1:n.1586C>T (COLQ)
ENST00000681097.1:c.*1135C>T (COLQ)	ENSP00000505397.1:n.*1135C>T
ENST00000681222.1:n.5612C>T (COLQ)
ENST00000383781.8:c.*753C>T (COLQ)	ENSP00000373291.3:n.*753C>T
ENST00000383788.9:c.*753C>T (COLQ)	ENSP00000373298.3:n.*753C>T
NM_005677.3:c.*753C>T (COLQ)	NP_005668.2:n.*753C>T
NM_080538.2:c.*753C>T (COLQ)	NP_536799.1:n.*753C>T
NM_080539.3:c.*753C>T (COLQ)	NP_536800.2:n.*753C>T
NM_005677.4:c.*753C>T (COLQ) MANE Select	NP_005668.2:n.*753C>T
NM_080539.4:c.*753C>T (COLQ)	NP_536800.2:n.*753C>T