Canonical Allele Identifier: CA2612399112

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9142050-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142054del , CM000673.2:g.9142054del	GRCh38
NC_000011.9:g.9163601del , CM000673.1:g.9163601del	GRCh37
NC_000011.8:g.9120177del	NCBI36
NG_053019.1:g.128285del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3569del MANE Select	ENSP00000328524.3:p.Asn1190ThrfsTer?
ENST00000525784.6:n.1431del
ENST00000530780.2:c.*3395del	ENSP00000433925.1:n.*3395del
ENST00000531747.2:n.3240del
ENST00000679446.1:n.3490del
ENST00000679458.1:n.4970del
ENST00000679460.1:n.4631del
ENST00000679568.1:c.3569del	ENSP00000505860.1:p.Asn1190ThrfsTer?
ENST00000679745.1:n.4074del
ENST00000679773.1:n.2730del
ENST00000679926.1:n.4871del
ENST00000679999.1:c.*626del	ENSP00000505198.1:n.*626del
ENST00000680252.1:c.3236del
ENST00000680294.1:c.3362del	ENSP00000506113.1:p.Asn1121ThrfsTer?
ENST00000680358.1:n.2868del
ENST00000680470.1:c.*1350del	ENSP00000505975.1:n.*1350del
ENST00000680554.1:c.*102del	ENSP00000505621.1:n.*102del
ENST00000680576.1:n.5045del
ENST00000680599.1:n.3610del
ENST00000680742.1:c.*102del	ENSP00000505206.1:n.*102del
ENST00000680791.1:n.2453del
ENST00000680885.1:n.5271del
ENST00000681158.1:c.3153del
ENST00000681203.1:c.3497del	ENSP00000506456.1:p.Asn1166ThrfsTer?
ENST00000681371.1:n.3441del
ENST00000681425.1:n.4047del
ENST00000681639.1:n.1848del
ENST00000328194.7:c.3569del	ENSP00000328524.3:p.Asn1190ThrfsTer?
ENST00000525784.5:c.505del
ENST00000527700.5:n.3131del
ENST00000528725.5:c.265del
ENST00000529977.5:n.1470del
ENST00000530044.5:c.3569del	ENSP00000435866.1:p.Asn1190ThrfsTer?
ENST00000531747.1:c.805del
ENST00000533737.5:c.232del
NM_001243254.1:c.3569del	NP_001230183.1:p.Asn1190ThrfsTer?
NM_015213.3:c.3569del	NP_056028.2:p.Asn1190ThrfsTer?
XM_005252832.1:c.3569del	XP_005252889.1:p.Asn1190ThrfsTer?
XM_011519952.1:c.3569del	XP_011518254.1:p.Asn1190ThrfsTer?
XM_011519953.1:c.1667del	XP_011518255.1:p.Asn556ThrfsTer?
XR_242782.2:n.3751del
XR_930851.1:n.3751del
NM_001348749.1:c.3497del	NP_001335678.1:p.Asn1166ThrfsTer?
NM_001348750.1:c.3281del	NP_001335679.1:p.Asn1094ThrfsTer?
NR_145966.2:n.3743del
NM_015213.4:c.3569del MANE Select	NP_056028.2:p.Asn1190ThrfsTer?
NM_001243254.2:c.3569del	NP_001230183.1:p.Asn1190ThrfsTer?
NM_001348749.2:c.3497del	NP_001335678.1:p.Asn1166ThrfsTer?
NM_001348750.2:c.3281del	NP_001335679.1:p.Asn1094ThrfsTer?