Canonical Allele Identifier: CA2612398895

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9141887-ACAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141896_9141898del , CM000673.2:g.9141896_9141898del	GRCh38
NC_000011.9:g.9163443_9163445del , CM000673.1:g.9163443_9163445del	GRCh37
NC_000011.8:g.9120019_9120021del	NCBI36
NG_053019.1:g.128446_128448del

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3680+50_3680+52del MANE Select	ENSP00000328524.3:n.3680+50_3680+52del
ENST00000525784.6:n.1542+50_1542+52del
ENST00000530780.2:c.*3506+50_*3506+52del	ENSP00000433925.1:n.*3506+50_*3506+52del
ENST00000531747.2:n.3351+50_3351+52del
ENST00000679446.1:n.3651_3653del
ENST00000679458.1:n.5081+50_5081+52del
ENST00000679460.1:n.4742+50_4742+52del
ENST00000679568.1:c.3680+50_3680+52del	ENSP00000505860.1:n.3680+50_3680+52del
ENST00000679745.1:n.4185+50_4185+52del
ENST00000679773.1:n.2841+50_2841+52del
ENST00000679926.1:n.4982+50_4982+52del
ENST00000679999.1:c.*737+50_*737+52del	ENSP00000505198.1:n.*737+50_*737+52del
ENST00000680252.1:c.3347+50_3347+52del
ENST00000680294.1:c.3473+50_3473+52del	ENSP00000506113.1:n.3473+50_3473+52del
ENST00000680358.1:n.2979+50_2979+52del
ENST00000680470.1:c.*1461+50_*1461+52del	ENSP00000505975.1:n.*1461+50_*1461+52del
ENST00000680554.1:c.*213+50_*213+52del	ENSP00000505621.1:n.*213+50_*213+52del
ENST00000680576.1:n.5206_5208del
ENST00000680599.1:n.3721+50_3721+52del
ENST00000680742.1:c.*179+84_*179+86del	ENSP00000505206.1:n.*179+84_*179+86del
ENST00000680791.1:n.2564+50_2564+52del
ENST00000680885.1:n.5382+50_5382+52del
ENST00000681158.1:c.3264+50_3264+52del
ENST00000681203.1:c.3608+50_3608+52del	ENSP00000506456.1:n.3608+50_3608+52del
ENST00000681371.1:n.3552+50_3552+52del
ENST00000681425.1:n.4158+50_4158+52del
ENST00000681639.1:n.1959+50_1959+52del
ENST00000328194.7:c.3680+50_3680+52del	ENSP00000328524.3:n.3680+50_3680+52del
ENST00000525784.5:c.616+50_616+52del
ENST00000527700.5:n.3242+50_3242+52del
ENST00000528725.5:c.376+50_376+52del
ENST00000529977.5:n.1581+50_1581+52del
ENST00000530044.5:c.3646+84_3646+86del	ENSP00000435866.1:n.3646+84_3646+86del
ENST00000533737.5:c.343+50_343+52del
NM_001243254.1:c.3646+84_3646+86del	NP_001230183.1:n.3646+84_3646+86del
NM_015213.3:c.3680+50_3680+52del	NP_056028.2:n.3680+50_3680+52del
XM_005252832.1:c.3680+50_3680+52del	XP_005252889.1:n.3680+50_3680+52del
XM_011519952.1:c.3646+84_3646+86del	XP_011518254.1:n.3646+84_3646+86del
XM_011519953.1:c.1778+50_1778+52del	XP_011518255.1:n.1778+50_1778+52del
XR_242782.2:n.3862+50_3862+52del
XR_930851.1:n.3828+84_3828+86del
NM_001348749.1:c.3608+50_3608+52del	NP_001335678.1:n.3608+50_3608+52del
NM_001348750.1:c.3392+50_3392+52del	NP_001335679.1:n.3392+50_3392+52del
NR_145966.2:n.3854+50_3854+52del
NM_015213.4:c.3680+50_3680+52del MANE Select	NP_056028.2:n.3680+50_3680+52del
NM_001243254.2:c.3646+84_3646+86del	NP_001230183.1:n.3646+84_3646+86del
NM_001348749.2:c.3608+50_3608+52del	NP_001335678.1:n.3608+50_3608+52del
NM_001348750.2:c.3392+50_3392+52del	NP_001335679.1:n.3392+50_3392+52del