Canonical Allele Identifier: CA1951453962
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9141809A= , CM000673.2:g.9141809A= GRCh38
NC_000011.9:g.9163356A= , CM000673.1:g.9163356A= GRCh37
NC_000011.8:g.9119932A= NCBI36
NG_053019.1:g.128527T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.3680+131T= MANE Select ENSP00000328524.3:n.3680+131T=
ENST00000525784.6:n.1542+131T=
ENST00000530780.2:c.*3506+131T= ENSP00000433925.1:n.*3506+131T=
ENST00000531747.2:n.3351+131T=
ENST00000679446.1:n.3732T=
ENST00000679458.1:n.5081+131T=
ENST00000679460.1:n.4742+131T=
ENST00000679568.1:c.3680+131T= ENSP00000505860.1:n.3680+131T=
ENST00000679745.1:n.4185+131T=
ENST00000679773.1:n.2841+131T=
ENST00000679926.1:n.4982+131T=
ENST00000679999.1:c.*737+131T= ENSP00000505198.1:n.*737+131T=
ENST00000680252.1:c.3347+131T=
ENST00000680294.1:c.3473+131T= ENSP00000506113.1:n.3473+131T=
ENST00000680358.1:n.2979+131T=
ENST00000680470.1:c.*1461+131T= ENSP00000505975.1:n.*1461+131T=
ENST00000680554.1:c.*213+131T= ENSP00000505621.1:n.*213+131T=
ENST00000680576.1:n.5287T=
ENST00000680599.1:n.3721+131T=
ENST00000680742.1:c.*179+165T= ENSP00000505206.1:n.*179+165T=
ENST00000680791.1:n.2564+131T=
ENST00000680885.1:n.5382+131T=
ENST00000681158.1:c.3264+131T=
ENST00000681203.1:c.3608+131T= ENSP00000506456.1:n.3608+131T=
ENST00000681371.1:n.3552+131T=
ENST00000681425.1:n.4158+131T=
ENST00000681639.1:n.1959+131T=
ENST00000328194.7:c.3680+131T= ENSP00000328524.3:n.3680+131T=
ENST00000525784.5:c.616+131T=
ENST00000527700.5:n.3242+131T=
ENST00000528725.5:c.376+131T=
ENST00000529977.5:n.1581+131T=
ENST00000530044.5:c.3646+165T= ENSP00000435866.1:n.3646+165T=
ENST00000533737.5:c.343+131T=
NM_001243254.1:c.3646+165T= NP_001230183.1:n.3646+165T=
NM_015213.3:c.3680+131T= NP_056028.2:n.3680+131T=
XM_005252832.1:c.3680+131T= XP_005252889.1:n.3680+131T=
XM_011519952.1:c.3646+165T= XP_011518254.1:n.3646+165T=
XM_011519953.1:c.1778+131T= XP_011518255.1:n.1778+131T=
XR_242782.2:n.3862+131T=
XR_930851.1:n.3828+165T=
NM_001348749.1:c.3608+131T= NP_001335678.1:n.3608+131T=
NM_001348750.1:c.3392+131T= NP_001335679.1:n.3392+131T=
NR_145966.2:n.3854+131T=
NM_015213.4:c.3680+131T= MANE Select NP_056028.2:n.3680+131T=
NM_001243254.2:c.3646+165T= NP_001230183.1:n.3646+165T=
NM_001348749.2:c.3608+131T= NP_001335678.1:n.3608+131T=
NM_001348750.2:c.3392+131T= NP_001335679.1:n.3392+131T=