Canonical Allele Identifier: CA2518764189
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9204397_9204401del , CM000673.2:g.9204397_9204401del GRCh38
NC_000011.9:g.9225944_9225948del , CM000673.1:g.9225944_9225948del GRCh37
NC_000011.8:g.9182520_9182524del NCBI36
NG_053019.1:g.65935_65939del

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.292-84_292-80del MANE Select ENSP00000328524.3:n.292-84_292-80del
ENST00000530780.2:c.*118-84_*118-80del ENSP00000433925.1:n.*118-84_*118-80del
ENST00000530867.2:n.81-84_81-80del
ENST00000532696.2:n.215-84_215-80del
ENST00000679446.1:n.213-84_213-80del
ENST00000679460.1:n.81-84_81-80del
ENST00000679568.1:c.292-84_292-80del ENSP00000505860.1:n.292-84_292-80del
ENST00000679745.1:n.81-84_81-80del
ENST00000679999.1:c.292-84_292-80del ENSP00000505198.1:n.292-84_292-80del
ENST00000680252.1:c.81-84_81-80del
ENST00000680294.1:c.292-84_292-80del ENSP00000506113.1:n.292-84_292-80del
ENST00000680470.1:c.292-84_292-80del ENSP00000505975.1:n.292-84_292-80del
ENST00000680554.1:c.4-84_4-80del ENSP00000505621.1:n.4-84_4-80del
ENST00000680576.1:n.81-84_81-80del
ENST00000680599.1:n.209-84_209-80del
ENST00000680742.1:c.292-84_292-80del ENSP00000505206.1:n.292-84_292-80del
ENST00000680885.1:n.213-84_213-80del
ENST00000681158.1:c.81-84_81-80del
ENST00000681173.1:n.81-84_81-80del
ENST00000681203.1:c.220-84_220-80del ENSP00000506456.1:n.220-84_220-80del
ENST00000681425.1:n.213-84_213-80del
ENST00000681915.1:n.81-84_81-80del
ENST00000328194.7:c.292-84_292-80del ENSP00000328524.3:n.292-84_292-80del
ENST00000526707.5:c.220-84_220-80del ENSP00000436780.1:n.220-84_220-80del
ENST00000530044.5:c.292-84_292-80del ENSP00000435866.1:n.292-84_292-80del
ENST00000530780.1:c.*118-84_*118-80del ENSP00000433925.1:n.*118-84_*118-80del
ENST00000532696.1:n.47-84_47-80del
NM_001243254.1:c.292-84_292-80del NP_001230183.1:n.292-84_292-80del
NM_015213.3:c.292-84_292-80del NP_056028.2:n.292-84_292-80del
XM_005252832.1:c.292-84_292-80del XP_005252889.1:n.292-84_292-80del
XM_011519952.1:c.292-84_292-80del XP_011518254.1:n.292-84_292-80del
XR_242782.2:n.557-84_557-80del
XR_930851.1:n.557-84_557-80del
XR_930852.1:n.557-84_557-80del
XR_930853.1:n.557-84_557-80del
NM_001348749.1:c.220-84_220-80del NP_001335678.1:n.220-84_220-80del
NM_001348750.1:c.4-84_4-80del NP_001335679.1:n.4-84_4-80del
NR_145966.2:n.549-84_549-80del
NM_015213.4:c.292-84_292-80del MANE Select NP_056028.2:n.292-84_292-80del
NM_001243254.2:c.292-84_292-80del NP_001230183.1:n.292-84_292-80del
NM_001348749.2:c.220-84_220-80del NP_001335678.1:n.220-84_220-80del
NM_001348750.2:c.4-84_4-80del NP_001335679.1:n.4-84_4-80del