Canonical Allele Identifier: CA379599036
Gene: DENND5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9204010G>T , CM000673.2:g.9204010G>T GRCh38
NC_000011.9:g.9225557G>T , CM000673.1:g.9225557G>T GRCh37
NC_000011.8:g.9182133G>T NCBI36
NG_053019.1:g.66326C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.599C>A MANE Select ENSP00000328524.3:p.Thr200Asn
ENST00000530780.2:c.*425C>A ENSP00000433925.1:n.*425C>A
ENST00000530867.2:n.388C>A
ENST00000532696.2:n.522C>A
ENST00000679446.1:n.520C>A
ENST00000679460.1:n.388C>A
ENST00000679568.1:c.599C>A ENSP00000505860.1:p.Thr200Asn
ENST00000679745.1:n.388C>A
ENST00000679999.1:c.599C>A ENSP00000505198.1:p.Thr200Asn
ENST00000680252.1:c.388C>A
ENST00000680294.1:c.599C>A ENSP00000506113.1:p.Thr200Asn
ENST00000680470.1:c.599C>A ENSP00000505975.1:p.Thr200Asn
ENST00000680554.1:c.311C>A ENSP00000505621.1:p.Thr104Asn
ENST00000680576.1:n.388C>A
ENST00000680599.1:n.516C>A
ENST00000680742.1:c.599C>A ENSP00000505206.1:p.Thr200Asn
ENST00000680885.1:n.520C>A
ENST00000681158.1:c.388C>A
ENST00000681173.1:n.388C>A
ENST00000681203.1:c.527C>A ENSP00000506456.1:p.Thr176Asn
ENST00000681425.1:n.520C>A
ENST00000681915.1:n.388C>A
ENST00000328194.7:c.599C>A ENSP00000328524.3:p.Thr200Asn
ENST00000526707.5:c.527C>A ENSP00000436780.1:p.Thr176Asn
ENST00000530044.5:c.599C>A ENSP00000435866.1:p.Thr200Asn
ENST00000532696.1:n.354C>A
NM_001243254.1:c.599C>A NP_001230183.1:p.Thr200Asn
NM_015213.3:c.599C>A NP_056028.2:p.Thr200Asn
XM_005252832.1:c.599C>A XP_005252889.1:p.Thr200Asn
XM_011519952.1:c.599C>A XP_011518254.1:p.Thr200Asn
XR_242782.2:n.864C>A
XR_930851.1:n.864C>A
XR_930852.1:n.864C>A
XR_930853.1:n.864C>A
NM_001348749.1:c.527C>A NP_001335678.1:p.Thr176Asn
NM_001348750.1:c.311C>A NP_001335679.1:p.Thr104Asn
NR_145966.2:n.856C>A
NM_015213.4:c.599C>A MANE Select NP_056028.2:p.Thr200Asn
NM_001243254.2:c.599C>A NP_001230183.1:p.Thr200Asn
NM_001348749.2:c.527C>A NP_001335678.1:p.Thr176Asn
NM_001348750.2:c.311C>A NP_001335679.1:p.Thr104Asn