Canonical Allele Identifier: CA1951492193

Gene: DENND5A

Linked Data

• dbSNP Id: rs1379831799
• gnomAD v4: 11-9204439-GCTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204444_9204447del , CM000673.2:g.9204444_9204447del	GRCh38
NC_000011.9:g.9225991_9225994del , CM000673.1:g.9225991_9225994del	GRCh37
NC_000011.8:g.9182567_9182570del	NCBI36
NG_053019.1:g.65893_65896del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.292-126_292-123del MANE Select	ENSP00000328524.3:n.292-126_292-123del
ENST00000530780.2:c.*118-126_*118-123del	ENSP00000433925.1:n.*118-126_*118-123del
ENST00000530867.2:n.81-126_81-123del
ENST00000532696.2:n.215-126_215-123del
ENST00000679446.1:n.213-126_213-123del
ENST00000679460.1:n.81-126_81-123del
ENST00000679568.1:c.292-126_292-123del	ENSP00000505860.1:n.292-126_292-123del
ENST00000679745.1:n.81-126_81-123del
ENST00000679999.1:c.292-126_292-123del	ENSP00000505198.1:n.292-126_292-123del
ENST00000680252.1:c.81-126_81-123del
ENST00000680294.1:c.292-126_292-123del	ENSP00000506113.1:n.292-126_292-123del
ENST00000680470.1:c.292-126_292-123del	ENSP00000505975.1:n.292-126_292-123del
ENST00000680554.1:c.4-126_4-123del	ENSP00000505621.1:n.4-126_4-123del
ENST00000680576.1:n.81-126_81-123del
ENST00000680599.1:n.209-126_209-123del
ENST00000680742.1:c.292-126_292-123del	ENSP00000505206.1:n.292-126_292-123del
ENST00000680885.1:n.213-126_213-123del
ENST00000681158.1:c.81-126_81-123del
ENST00000681173.1:n.81-126_81-123del
ENST00000681203.1:c.220-126_220-123del	ENSP00000506456.1:n.220-126_220-123del
ENST00000681425.1:n.213-126_213-123del
ENST00000681915.1:n.81-126_81-123del
ENST00000328194.7:c.292-126_292-123del	ENSP00000328524.3:n.292-126_292-123del
ENST00000526707.5:c.220-126_220-123del	ENSP00000436780.1:n.220-126_220-123del
ENST00000530044.5:c.292-126_292-123del	ENSP00000435866.1:n.292-126_292-123del
ENST00000530780.1:c.*118-126_*118-123del	ENSP00000433925.1:n.*118-126_*118-123del
ENST00000532696.1:n.47-126_47-123del
NM_001243254.1:c.292-126_292-123del	NP_001230183.1:n.292-126_292-123del
NM_015213.3:c.292-126_292-123del	NP_056028.2:n.292-126_292-123del
XM_005252832.1:c.292-126_292-123del	XP_005252889.1:n.292-126_292-123del
XM_011519952.1:c.292-126_292-123del	XP_011518254.1:n.292-126_292-123del
XR_242782.2:n.557-126_557-123del
XR_930851.1:n.557-126_557-123del
XR_930852.1:n.557-126_557-123del
XR_930853.1:n.557-126_557-123del
NM_001348749.1:c.220-126_220-123del	NP_001335678.1:n.220-126_220-123del
NM_001348750.1:c.4-126_4-123del	NP_001335679.1:n.4-126_4-123del
NR_145966.2:n.549-126_549-123del
NM_015213.4:c.292-126_292-123del MANE Select	NP_056028.2:n.292-126_292-123del
NM_001243254.2:c.292-126_292-123del	NP_001230183.1:n.292-126_292-123del
NM_001348749.2:c.220-126_220-123del	NP_001335678.1:n.220-126_220-123del
NM_001348750.2:c.4-126_4-123del	NP_001335679.1:n.4-126_4-123del