Canonical Allele Identifier: CA900927111

Gene: EAF1-AS1 COLQ

Linked Data

• dbSNP Id: rs1317390473
• MyVariant Identifiers: chr3:g.15492292A>G (hg19) ; chr3:g.15450785A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15450785A>G , CM000665.2:g.15450785A>G	GRCh38
NC_000003.11:g.15492292A>G , CM000665.1:g.15492292A>G	GRCh37
NC_000003.10:g.15467296A>G	NCBI36
NG_009032.1:g.75967T>C
NG_009032.2:g.75967T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000608408.2:n.398+660T>C (EAF1-AS1)
ENST00000626521.1:n.55+660T>C (EAF1-AS1)
ENST00000629729.3:c.414+660T>C	ENSP00000518887.1:n.414+660T>C
ENST00000383788.10:c.*859T>C (COLQ) MANE Select	ENSP00000373298.3:n.*859T>C
ENST00000679838.1:c.*1989T>C (COLQ)	ENSP00000505708.1:n.*1989T>C
ENST00000680545.1:n.1993T>C (COLQ)
ENST00000680897.1:n.1692T>C (COLQ)
ENST00000681097.1:c.*1241T>C (COLQ)	ENSP00000505397.1:n.*1241T>C
ENST00000681222.1:n.5718T>C (COLQ)
ENST00000383781.8:c.*859T>C (COLQ)	ENSP00000373291.3:n.*859T>C
ENST00000383788.9:c.*859T>C (COLQ)	ENSP00000373298.3:n.*859T>C
ENST00000603752.1:n.95T>C (COLQ)
NM_005677.3:c.*859T>C (COLQ)	NP_005668.2:n.*859T>C
NM_080538.2:c.*859T>C (COLQ)	NP_536799.1:n.*859T>C
NM_080539.3:c.*859T>C (COLQ)	NP_536800.2:n.*859T>C
NM_005677.4:c.*859T>C (COLQ) MANE Select	NP_005668.2:n.*859T>C
NM_080539.4:c.*859T>C (COLQ)	NP_536800.2:n.*859T>C