Canonical Allele Identifier: CA1951492192

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204439_9204443delinsGCTCT , CM000673.2:g.9204439_9204443delinsGCTCT	GRCh38
NC_000011.9:g.9225986_9225990delinsGCTCT , CM000673.1:g.9225986_9225990delinsGCTCT	GRCh37
NC_000011.8:g.9182562_9182566delinsGCTCT	NCBI36
NG_053019.1:g.65893_65897delinsAGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.292-126_292-122delinsAGAGC MANE Select	ENSP00000328524.3:n.292-126_292-122delinsAGAGC
ENST00000530780.2:c.*118-126_*118-122delinsAGAGC	ENSP00000433925.1:n.*118-126_*118-122delinsAGAGC
ENST00000530867.2:n.81-126_81-122delinsAGAGC
ENST00000532696.2:n.215-126_215-122delinsAGAGC
ENST00000679446.1:n.213-126_213-122delinsAGAGC
ENST00000679460.1:n.81-126_81-122delinsAGAGC
ENST00000679568.1:c.292-126_292-122delinsAGAGC	ENSP00000505860.1:n.292-126_292-122delinsAGAGC
ENST00000679745.1:n.81-126_81-122delinsAGAGC
ENST00000679999.1:c.292-126_292-122delinsAGAGC	ENSP00000505198.1:n.292-126_292-122delinsAGAGC
ENST00000680252.1:c.81-126_81-122delinsAGAGC
ENST00000680294.1:c.292-126_292-122delinsAGAGC	ENSP00000506113.1:n.292-126_292-122delinsAGAGC
ENST00000680470.1:c.292-126_292-122delinsAGAGC	ENSP00000505975.1:n.292-126_292-122delinsAGAGC
ENST00000680554.1:c.4-126_4-122delinsAGAGC	ENSP00000505621.1:n.4-126_4-122delinsAGAGC
ENST00000680576.1:n.81-126_81-122delinsAGAGC
ENST00000680599.1:n.209-126_209-122delinsAGAGC
ENST00000680742.1:c.292-126_292-122delinsAGAGC	ENSP00000505206.1:n.292-126_292-122delinsAGAGC
ENST00000680885.1:n.213-126_213-122delinsAGAGC
ENST00000681158.1:c.81-126_81-122delinsAGAGC
ENST00000681173.1:n.81-126_81-122delinsAGAGC
ENST00000681203.1:c.220-126_220-122delinsAGAGC	ENSP00000506456.1:n.220-126_220-122delinsAGAGC
ENST00000681425.1:n.213-126_213-122delinsAGAGC
ENST00000681915.1:n.81-126_81-122delinsAGAGC
ENST00000328194.7:c.292-126_292-122delinsAGAGC	ENSP00000328524.3:n.292-126_292-122delinsAGAGC
ENST00000526707.5:c.220-126_220-122delinsAGAGC	ENSP00000436780.1:n.220-126_220-122delinsAGAGC
ENST00000530044.5:c.292-126_292-122delinsAGAGC	ENSP00000435866.1:n.292-126_292-122delinsAGAGC
ENST00000530780.1:c.*118-126_*118-122delinsAGAGC	ENSP00000433925.1:n.*118-126_*118-122delinsAGAGC
ENST00000532696.1:n.47-126_47-122delinsAGAGC
NM_001243254.1:c.292-126_292-122delinsAGAGC	NP_001230183.1:n.292-126_292-122delinsAGAGC
NM_015213.3:c.292-126_292-122delinsAGAGC	NP_056028.2:n.292-126_292-122delinsAGAGC
XM_005252832.1:c.292-126_292-122delinsAGAGC	XP_005252889.1:n.292-126_292-122delinsAGAGC
XM_011519952.1:c.292-126_292-122delinsAGAGC	XP_011518254.1:n.292-126_292-122delinsAGAGC
XR_242782.2:n.557-126_557-122delinsAGAGC
XR_930851.1:n.557-126_557-122delinsAGAGC
XR_930852.1:n.557-126_557-122delinsAGAGC
XR_930853.1:n.557-126_557-122delinsAGAGC
NM_001348749.1:c.220-126_220-122delinsAGAGC	NP_001335678.1:n.220-126_220-122delinsAGAGC
NM_001348750.1:c.4-126_4-122delinsAGAGC	NP_001335679.1:n.4-126_4-122delinsAGAGC
NR_145966.2:n.549-126_549-122delinsAGAGC
NM_015213.4:c.292-126_292-122delinsAGAGC MANE Select	NP_056028.2:n.292-126_292-122delinsAGAGC
NM_001243254.2:c.292-126_292-122delinsAGAGC	NP_001230183.1:n.292-126_292-122delinsAGAGC
NM_001348749.2:c.220-126_220-122delinsAGAGC	NP_001335678.1:n.220-126_220-122delinsAGAGC
NM_001348750.2:c.4-126_4-122delinsAGAGC	NP_001335679.1:n.4-126_4-122delinsAGAGC