Canonical Allele Identifier: CA1951464148
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9160502_9160508delinsAAAAGTC , CM000673.2:g.9160502_9160508delinsAAAAGTC GRCh38
NC_000011.9:g.9182049_9182055delinsAAAAGTC , CM000673.1:g.9182049_9182055delinsAAAAGTC GRCh37
NC_000011.8:g.9138625_9138631delinsAAAAGTC NCBI36
NG_053019.1:g.109828_109834delinsGACTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.2436+205_2436+211delinsGACTTTT MANE Select ENSP00000328524.3:n.2436+205_2436+211delinsGACTTTT
ENST00000530780.2:c.*2262+205_*2262+211delinsGACTTTT ENSP00000433925.1:n.*2262+205_*2262+211delinsGACTTTT
ENST00000679446.1:n.2357+205_2357+211delinsGACTTTT
ENST00000679458.1:n.3837+205_3837+211delinsGACTTTT
ENST00000679460.1:n.2225+205_2225+211delinsGACTTTT
ENST00000679568.1:c.2436+205_2436+211delinsGACTTTT ENSP00000505860.1:n.2436+205_2436+211delinsGACTTTT
ENST00000679745.1:n.2225+205_2225+211delinsGACTTTT
ENST00000679926.1:n.1252+205_1252+211delinsGACTTTT
ENST00000679999.1:c.2436+205_2436+211delinsGACTTTT ENSP00000505198.1:n.2436+205_2436+211delinsGACTTTT
ENST00000680252.1:c.2225+205_2225+211delinsGACTTTT
ENST00000680294.1:c.2436+205_2436+211delinsGACTTTT ENSP00000506113.1:n.2436+205_2436+211delinsGACTTTT
ENST00000680358.1:n.1735+205_1735+211delinsGACTTTT
ENST00000680470.1:c.*302+205_*302+211delinsGACTTTT ENSP00000505975.1:n.*302+205_*302+211delinsGACTTTT
ENST00000680554.1:c.2148+205_2148+211delinsGACTTTT ENSP00000505621.1:n.2148+205_2148+211delinsGACTTTT
ENST00000680576.1:n.2225+205_2225+211delinsGACTTTT
ENST00000680599.1:n.2353+205_2353+211delinsGACTTTT
ENST00000680742.1:c.2436+205_2436+211delinsGACTTTT ENSP00000505206.1:n.2436+205_2436+211delinsGACTTTT
ENST00000680885.1:n.2357+205_2357+211delinsGACTTTT
ENST00000681158.1:c.2225+205_2225+211delinsGACTTTT
ENST00000681173.1:n.2225+205_2226-203delinsGACTTTT
ENST00000681203.1:c.2364+205_2364+211delinsGACTTTT ENSP00000506456.1:n.2364+205_2364+211delinsGACTTTT
ENST00000681425.1:n.2357+205_2357+211delinsGACTTTT
ENST00000328194.7:c.2436+205_2436+211delinsGACTTTT ENSP00000328524.3:n.2436+205_2436+211delinsGACTTTT
ENST00000526707.5:c.2364+205_2364+211delinsGACTTTT ENSP00000436780.1:n.2364+205_2364+211delinsGACTTTT
ENST00000527700.5:n.1998+205_1998+211delinsGACTTTT
ENST00000530044.5:c.2436+205_2436+211delinsGACTTTT ENSP00000435866.1:n.2436+205_2436+211delinsGACTTTT
NM_001243254.1:c.2436+205_2436+211delinsGACTTTT NP_001230183.1:n.2436+205_2436+211delinsGACTTTT
NM_015213.3:c.2436+205_2436+211delinsGACTTTT NP_056028.2:n.2436+205_2436+211delinsGACTTTT
XM_005252832.1:c.2436+205_2436+211delinsGACTTTT XP_005252889.1:n.2436+205_2436+211delinsGACTTTT
XM_011519952.1:c.2436+205_2436+211delinsGACTTTT XP_011518254.1:n.2436+205_2436+211delinsGACTTTT
XM_011519953.1:c.534+205_534+211delinsGACTTTT XP_011518255.1:n.534+205_534+211delinsGACTTTT
XR_242782.2:n.2701+205_2701+211delinsGACTTTT
XR_930851.1:n.2701+205_2701+211delinsGACTTTT
XR_930852.1:n.2701+205_2701+211delinsGACTTTT
XR_930853.1:n.2550+205_2550+211delinsGACTTTT
NM_001348749.1:c.2364+205_2364+211delinsGACTTTT NP_001335678.1:n.2364+205_2364+211delinsGACTTTT
NM_001348750.1:c.2148+205_2148+211delinsGACTTTT NP_001335679.1:n.2148+205_2148+211delinsGACTTTT
NR_145966.2:n.2693+205_2693+211delinsGACTTTT
NM_015213.4:c.2436+205_2436+211delinsGACTTTT MANE Select NP_056028.2:n.2436+205_2436+211delinsGACTTTT
NM_001243254.2:c.2436+205_2436+211delinsGACTTTT NP_001230183.1:n.2436+205_2436+211delinsGACTTTT
NM_001348749.2:c.2364+205_2364+211delinsGACTTTT NP_001335678.1:n.2364+205_2364+211delinsGACTTTT
NM_001348750.2:c.2148+205_2148+211delinsGACTTTT NP_001335679.1:n.2148+205_2148+211delinsGACTTTT