Canonical Allele Identifier: CA2612399028

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9141991-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141995del , CM000673.2:g.9141995del	GRCh38
NC_000011.9:g.9163542del , CM000673.1:g.9163542del	GRCh37
NC_000011.8:g.9120118del	NCBI36
NG_053019.1:g.128344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3628del MANE Select	ENSP00000328524.3:p.Arg1210GlyfsTer?
ENST00000525784.6:n.1490del
ENST00000530780.2:c.*3454del	ENSP00000433925.1:n.*3454del
ENST00000531747.2:n.3299del
ENST00000679446.1:n.3549del
ENST00000679458.1:n.5029del
ENST00000679460.1:n.4690del
ENST00000679568.1:c.3628del	ENSP00000505860.1:p.Arg1210GlyfsTer21
ENST00000679745.1:n.4133del
ENST00000679773.1:n.2789del
ENST00000679926.1:n.4930del
ENST00000679999.1:c.*685del	ENSP00000505198.1:n.*685del
ENST00000680252.1:c.3295del
ENST00000680294.1:c.3421del	ENSP00000506113.1:p.Arg1141GlyfsTer?
ENST00000680358.1:n.2927del
ENST00000680470.1:c.*1409del	ENSP00000505975.1:n.*1409del
ENST00000680554.1:c.*161del	ENSP00000505621.1:n.*161del
ENST00000680576.1:n.5104del
ENST00000680599.1:n.3669del
ENST00000680742.1:c.*161del	ENSP00000505206.1:n.*161del
ENST00000680791.1:n.2512del
ENST00000680885.1:n.5330del
ENST00000681158.1:c.3212del
ENST00000681203.1:c.3556del	ENSP00000506456.1:p.Arg1186GlyfsTer?
ENST00000681371.1:n.3500del
ENST00000681425.1:n.4106del
ENST00000681639.1:n.1907del
ENST00000328194.7:c.3628del	ENSP00000328524.3:p.Arg1210GlyfsTer?
ENST00000525784.5:c.564del
ENST00000527700.5:n.3190del
ENST00000528725.5:c.324del
ENST00000529977.5:n.1529del
ENST00000530044.5:c.3628del	ENSP00000435866.1:p.Arg1210GlyfsTer19
ENST00000531747.1:c.864del
ENST00000533737.5:c.291del
NM_001243254.1:c.3628del	NP_001230183.1:p.Arg1210GlyfsTer19
NM_015213.3:c.3628del	NP_056028.2:p.Arg1210GlyfsTer?
XM_005252832.1:c.3628del	XP_005252889.1:p.Arg1210GlyfsTer21
XM_011519952.1:c.3628del	XP_011518254.1:p.Arg1210GlyfsTer12
XM_011519953.1:c.1726del	XP_011518255.1:p.Arg576GlyfsTer21
XR_242782.2:n.3810del
XR_930851.1:n.3810del
NM_001348749.1:c.3556del	NP_001335678.1:p.Arg1186GlyfsTer?
NM_001348750.1:c.3340del	NP_001335679.1:p.Arg1114GlyfsTer?
NR_145966.2:n.3802del
NM_015213.4:c.3628del MANE Select	NP_056028.2:p.Arg1210GlyfsTer?
NM_001243254.2:c.3628del	NP_001230183.1:p.Arg1210GlyfsTer19
NM_001348749.2:c.3556del	NP_001335678.1:p.Arg1186GlyfsTer?
NM_001348750.2:c.3340del	NP_001335679.1:p.Arg1114GlyfsTer?