Canonical Allele Identifier: CA2612397960

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9139631-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9139633_9139634del , CM000673.2:g.9139633_9139634del	GRCh38
NC_000011.9:g.9161180_9161181del , CM000673.1:g.9161180_9161181del	GRCh37
NC_000011.8:g.9117756_9117757del	NCBI36
NG_053019.1:g.130703_130704del

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.*38_*39del MANE Select	ENSP00000328524.3:n.*38_*39del
ENST00000525784.6:n.1764_1765del
ENST00000530780.2:c.*3728_*3729del	ENSP00000433925.1:n.*3728_*3729del
ENST00000531747.2:n.3573_3574del
ENST00000679446.1:n.5908_5909del
ENST00000679458.1:n.5303_5304del
ENST00000679460.1:n.4964_4965del
ENST00000679568.1:c.*38_*39del	ENSP00000505860.1:n.*38_*39del
ENST00000679745.1:n.4407_4408del
ENST00000679773.1:n.3063_3064del
ENST00000679926.1:n.5204_5205del
ENST00000679999.1:c.*959_*960del	ENSP00000505198.1:n.*959_*960del
ENST00000680252.1:c.3569_3570del
ENST00000680294.1:c.*38_*39del	ENSP00000506113.1:n.*38_*39del
ENST00000680358.1:n.3201_3202del
ENST00000680470.1:c.*1683_*1684del	ENSP00000505975.1:n.*1683_*1684del
ENST00000680554.1:c.*435_*436del	ENSP00000505621.1:n.*435_*436del
ENST00000680576.1:n.7463_7464del
ENST00000680599.1:n.3943_3944del
ENST00000680742.1:c.*401_*402del	ENSP00000505206.1:n.*401_*402del
ENST00000680791.1:n.2786_2787del
ENST00000680885.1:n.5604_5605del
ENST00000681158.1:c.3486_3487del
ENST00000681203.1:c.*38_*39del	ENSP00000506456.1:n.*38_*39del
ENST00000681371.1:n.3774_3775del
ENST00000681425.1:n.4380_4381del
ENST00000681639.1:n.2181_2182del
ENST00000328194.7:c.*38_*39del	ENSP00000328524.3:n.*38_*39del
ENST00000527700.5:n.3464_3465del
ENST00000528725.5:c.598_599del
ENST00000529977.5:n.1803_1804del
ENST00000530044.5:c.*142_*143del	ENSP00000435866.1:n.*142_*143del
ENST00000533737.5:c.625_626del
NM_001243254.1:c.*142_*143del	NP_001230183.1:n.*142_*143del
NM_015213.3:c.*38_*39del	NP_056028.2:n.*38_*39del
XM_005252832.1:c.*38_*39del	XP_005252889.1:n.*38_*39del
XM_011519953.1:c.*38_*39del	XP_011518255.1:n.*38_*39del
XR_242782.2:n.4084_4085del
XR_930851.1:n.4050_4051del
NM_001348749.1:c.*38_*39del	NP_001335678.1:n.*38_*39del
NM_001348750.1:c.*38_*39del	NP_001335679.1:n.*38_*39del
NR_145966.2:n.4076_4077del
NM_015213.4:c.*38_*39del MANE Select	NP_056028.2:n.*38_*39del
NM_001243254.2:c.*142_*143del	NP_001230183.1:n.*142_*143del
NM_001348749.2:c.*38_*39del	NP_001335678.1:n.*38_*39del
NM_001348750.2:c.*38_*39del	NP_001335679.1:n.*38_*39del