Canonical Allele Identifier: CA2612399178
Gene: DENND5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9142175del , CM000673.2:g.9142175del GRCh38
NC_000011.9:g.9163722del , CM000673.1:g.9163722del GRCh37
NC_000011.8:g.9120298del NCBI36
NG_053019.1:g.128162del

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.3512-66del MANE Select ENSP00000328524.3:n.3512-66del
ENST00000525784.6:n.1374-66del
ENST00000530780.2:c.*3338-66del ENSP00000433925.1:n.*3338-66del
ENST00000531747.2:n.3183-66del
ENST00000679446.1:n.3433-66del
ENST00000679458.1:n.4913-66del
ENST00000679460.1:n.4574-66del
ENST00000679568.1:c.3512-66del ENSP00000505860.1:n.3512-66del
ENST00000679745.1:n.4017-66del
ENST00000679773.1:n.2673-66del
ENST00000679926.1:n.4814-66del
ENST00000679999.1:c.*569-66del ENSP00000505198.1:n.*569-66del
ENST00000680252.1:c.3179-66del
ENST00000680294.1:c.3305-66del ENSP00000506113.1:n.3305-66del
ENST00000680358.1:n.2811-66del
ENST00000680470.1:c.*1293-66del ENSP00000505975.1:n.*1293-66del
ENST00000680554.1:c.*45-66del ENSP00000505621.1:n.*45-66del
ENST00000680576.1:n.4988-66del
ENST00000680599.1:n.3553-66del
ENST00000680742.1:c.*45-66del ENSP00000505206.1:n.*45-66del
ENST00000680791.1:n.2396-66del
ENST00000680885.1:n.5148del
ENST00000681158.1:c.3096-66del
ENST00000681203.1:c.3440-66del ENSP00000506456.1:n.3440-66del
ENST00000681371.1:n.3384-66del
ENST00000681425.1:n.3990-66del
ENST00000681639.1:n.1725del
ENST00000328194.7:c.3512-66del ENSP00000328524.3:n.3512-66del
ENST00000525784.5:c.448-66del
ENST00000527700.5:n.3074-66del
ENST00000528725.5:c.208-66del
ENST00000529977.5:n.1413-66del
ENST00000530044.5:c.3512-66del ENSP00000435866.1:n.3512-66del
ENST00000531747.1:c.748-66del
ENST00000533737.5:c.175-66del
NM_001243254.1:c.3512-66del NP_001230183.1:n.3512-66del
NM_015213.3:c.3512-66del NP_056028.2:n.3512-66del
XM_005252832.1:c.3512-66del XP_005252889.1:n.3512-66del
XM_011519952.1:c.3512-66del XP_011518254.1:n.3512-66del
XM_011519953.1:c.1610-66del XP_011518255.1:n.1610-66del
XR_242782.2:n.3694-66del
XR_930851.1:n.3694-66del
NM_001348749.1:c.3440-66del NP_001335678.1:n.3440-66del
NM_001348750.1:c.3224-66del NP_001335679.1:n.3224-66del
NR_145966.2:n.3686-66del
NM_015213.4:c.3512-66del MANE Select NP_056028.2:n.3512-66del
NM_001243254.2:c.3512-66del NP_001230183.1:n.3512-66del
NM_001348749.2:c.3440-66del NP_001335678.1:n.3440-66del
NM_001348750.2:c.3224-66del NP_001335679.1:n.3224-66del