Canonical Allele Identifier: CA10617756

Gene: EAF1-AS1 COLQ

Linked Data

• ClinVar Variation Id: 343834
• ClinVar RCV Id: RCV000396412
• dbSNP Id: rs544927968
• gnomAD v2: 3-15492635-C-T
• gnomAD v3: 3-15451128-C-T
• gnomAD v4: 3-15451128-C-T
• MyVariant Identifiers: chr3:g.15492635C>T (hg19) ; chr3:g.15451128C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.15451128C>T , CM000665.2:g.15451128C>T	GRCh38
NC_000003.11:g.15492635C>T , CM000665.1:g.15492635C>T	GRCh37
NC_000003.10:g.15467639C>T	NCBI36
NG_009032.1:g.75624G>A
NG_009032.2:g.75624G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000608408.2:n.398+317G>A (EAF1-AS1)
ENST00000626521.1:n.55+317G>A (EAF1-AS1)
ENST00000629729.3:c.414+317G>A	ENSP00000518887.1:n.414+317G>A
ENST00000383788.10:c.*516G>A (COLQ) MANE Select	ENSP00000373298.3:n.*516G>A
ENST00000604401.2:n.1740G>A (COLQ)
ENST00000679838.1:c.*1646G>A (COLQ)	ENSP00000505708.1:n.*1646G>A
ENST00000680545.1:n.1650G>A (COLQ)
ENST00000680897.1:n.1349G>A (COLQ)
ENST00000681097.1:c.*898G>A (COLQ)	ENSP00000505397.1:n.*898G>A
ENST00000681222.1:n.5375G>A (COLQ)
ENST00000383781.8:c.*516G>A (COLQ)	ENSP00000373291.3:n.*516G>A
ENST00000383788.9:c.*516G>A (COLQ)	ENSP00000373298.3:n.*516G>A
NM_005677.3:c.*516G>A (COLQ)	NP_005668.2:n.*516G>A
NM_080538.2:c.*516G>A (COLQ)	NP_536799.1:n.*516G>A
NM_080539.3:c.*516G>A (COLQ)	NP_536800.2:n.*516G>A
NM_005677.4:c.*516G>A (COLQ) MANE Select	NP_005668.2:n.*516G>A
NM_080539.4:c.*516G>A (COLQ)	NP_536800.2:n.*516G>A