Canonical Allele Identifier: CA2612398819

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9141820-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141822del , CM000673.2:g.9141822del	GRCh38
NC_000011.9:g.9163369del , CM000673.1:g.9163369del	GRCh37
NC_000011.8:g.9119945del	NCBI36
NG_053019.1:g.128515del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+119del MANE Select	ENSP00000328524.3:n.3680+119del
ENST00000525784.6:n.1542+119del
ENST00000530780.2:c.*3506+119del	ENSP00000433925.1:n.*3506+119del
ENST00000531747.2:n.3351+119del
ENST00000679446.1:n.3720del
ENST00000679458.1:n.5081+119del
ENST00000679460.1:n.4742+119del
ENST00000679568.1:c.3680+119del	ENSP00000505860.1:n.3680+119del
ENST00000679745.1:n.4185+119del
ENST00000679773.1:n.2841+119del
ENST00000679926.1:n.4982+119del
ENST00000679999.1:c.*737+119del	ENSP00000505198.1:n.*737+119del
ENST00000680252.1:c.3347+119del
ENST00000680294.1:c.3473+119del	ENSP00000506113.1:n.3473+119del
ENST00000680358.1:n.2979+119del
ENST00000680470.1:c.*1461+119del	ENSP00000505975.1:n.*1461+119del
ENST00000680554.1:c.*213+119del	ENSP00000505621.1:n.*213+119del
ENST00000680576.1:n.5275del
ENST00000680599.1:n.3721+119del
ENST00000680742.1:c.*179+153del	ENSP00000505206.1:n.*179+153del
ENST00000680791.1:n.2564+119del
ENST00000680885.1:n.5382+119del
ENST00000681158.1:c.3264+119del
ENST00000681203.1:c.3608+119del	ENSP00000506456.1:n.3608+119del
ENST00000681371.1:n.3552+119del
ENST00000681425.1:n.4158+119del
ENST00000681639.1:n.1959+119del
ENST00000328194.7:c.3680+119del	ENSP00000328524.3:n.3680+119del
ENST00000525784.5:c.616+119del
ENST00000527700.5:n.3242+119del
ENST00000528725.5:c.376+119del
ENST00000529977.5:n.1581+119del
ENST00000530044.5:c.3646+153del	ENSP00000435866.1:n.3646+153del
ENST00000533737.5:c.343+119del
NM_001243254.1:c.3646+153del	NP_001230183.1:n.3646+153del
NM_015213.3:c.3680+119del	NP_056028.2:n.3680+119del
XM_005252832.1:c.3680+119del	XP_005252889.1:n.3680+119del
XM_011519952.1:c.3646+153del	XP_011518254.1:n.3646+153del
XM_011519953.1:c.1778+119del	XP_011518255.1:n.1778+119del
XR_242782.2:n.3862+119del
XR_930851.1:n.3828+153del
NM_001348749.1:c.3608+119del	NP_001335678.1:n.3608+119del
NM_001348750.1:c.3392+119del	NP_001335679.1:n.3392+119del
NR_145966.2:n.3854+119del
NM_015213.4:c.3680+119del MANE Select	NP_056028.2:n.3680+119del
NM_001243254.2:c.3646+153del	NP_001230183.1:n.3646+153del
NM_001348749.2:c.3608+119del	NP_001335678.1:n.3608+119del
NM_001348750.2:c.3392+119del	NP_001335679.1:n.3392+119del