Canonical Allele Identifier: CA2612398906

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9141900-GGCTAACCGCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141902_9141911del , CM000673.2:g.9141902_9141911del	GRCh38
NC_000011.9:g.9163449_9163458del , CM000673.1:g.9163449_9163458del	GRCh37
NC_000011.8:g.9120025_9120034del	NCBI36
NG_053019.1:g.128426_128435del

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3680+30_3680+39del MANE Select	ENSP00000328524.3:n.3680+30_3680+39del
ENST00000525784.6:n.1542+30_1542+39del
ENST00000530780.2:c.*3506+30_*3506+39del	ENSP00000433925.1:n.*3506+30_*3506+39del
ENST00000531747.2:n.3351+30_3351+39del
ENST00000679446.1:n.3631_3640del
ENST00000679458.1:n.5081+30_5081+39del
ENST00000679460.1:n.4742+30_4742+39del
ENST00000679568.1:c.3680+30_3680+39del	ENSP00000505860.1:n.3680+30_3680+39del
ENST00000679745.1:n.4185+30_4185+39del
ENST00000679773.1:n.2841+30_2841+39del
ENST00000679926.1:n.4982+30_4982+39del
ENST00000679999.1:c.*737+30_*737+39del	ENSP00000505198.1:n.*737+30_*737+39del
ENST00000680252.1:c.3347+30_3347+39del
ENST00000680294.1:c.3473+30_3473+39del	ENSP00000506113.1:n.3473+30_3473+39del
ENST00000680358.1:n.2979+30_2979+39del
ENST00000680470.1:c.*1461+30_*1461+39del	ENSP00000505975.1:n.*1461+30_*1461+39del
ENST00000680554.1:c.*213+30_*213+39del	ENSP00000505621.1:n.*213+30_*213+39del
ENST00000680576.1:n.5186_5195del
ENST00000680599.1:n.3721+30_3721+39del
ENST00000680742.1:c.*179+64_*179+73del	ENSP00000505206.1:n.*179+64_*179+73del
ENST00000680791.1:n.2564+30_2564+39del
ENST00000680885.1:n.5382+30_5382+39del
ENST00000681158.1:c.3264+30_3264+39del
ENST00000681203.1:c.3608+30_3608+39del	ENSP00000506456.1:n.3608+30_3608+39del
ENST00000681371.1:n.3552+30_3552+39del
ENST00000681425.1:n.4158+30_4158+39del
ENST00000681639.1:n.1959+30_1959+39del
ENST00000328194.7:c.3680+30_3680+39del	ENSP00000328524.3:n.3680+30_3680+39del
ENST00000525784.5:c.616+30_616+39del
ENST00000527700.5:n.3242+30_3242+39del
ENST00000528725.5:c.376+30_376+39del
ENST00000529977.5:n.1581+30_1581+39del
ENST00000530044.5:c.3646+64_3646+73del	ENSP00000435866.1:n.3646+64_3646+73del
ENST00000533737.5:c.343+30_343+39del
NM_001243254.1:c.3646+64_3646+73del	NP_001230183.1:n.3646+64_3646+73del
NM_015213.3:c.3680+30_3680+39del	NP_056028.2:n.3680+30_3680+39del
XM_005252832.1:c.3680+30_3680+39del	XP_005252889.1:n.3680+30_3680+39del
XM_011519952.1:c.3646+64_3646+73del	XP_011518254.1:n.3646+64_3646+73del
XM_011519953.1:c.1778+30_1778+39del	XP_011518255.1:n.1778+30_1778+39del
XR_242782.2:n.3862+30_3862+39del
XR_930851.1:n.3828+64_3828+73del
NM_001348749.1:c.3608+30_3608+39del	NP_001335678.1:n.3608+30_3608+39del
NM_001348750.1:c.3392+30_3392+39del	NP_001335679.1:n.3392+30_3392+39del
NR_145966.2:n.3854+30_3854+39del
NM_015213.4:c.3680+30_3680+39del MANE Select	NP_056028.2:n.3680+30_3680+39del
NM_001243254.2:c.3646+64_3646+73del	NP_001230183.1:n.3646+64_3646+73del
NM_001348749.2:c.3608+30_3608+39del	NP_001335678.1:n.3608+30_3608+39del
NM_001348750.2:c.3392+30_3392+39del	NP_001335679.1:n.3392+30_3392+39del