Canonical Allele Identifier: CA1951491953
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9203930G= , CM000673.2:g.9203930G= GRCh38
NC_000011.9:g.9225477G= , CM000673.1:g.9225477G= GRCh37
NC_000011.8:g.9182053G= NCBI36
NG_053019.1:g.66406C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.679C= MANE Select ENSP00000328524.3:p.His227=
ENST00000530780.2:c.*505C= ENSP00000433925.1:n.*505C=
ENST00000530867.2:n.468C=
ENST00000532696.2:n.602C=
ENST00000679446.1:n.600C=
ENST00000679460.1:n.468C=
ENST00000679568.1:c.679C= ENSP00000505860.1:p.His227=
ENST00000679745.1:n.468C=
ENST00000679999.1:c.679C= ENSP00000505198.1:p.His227=
ENST00000680252.1:c.468C=
ENST00000680294.1:c.679C= ENSP00000506113.1:p.His227=
ENST00000680470.1:c.679C= ENSP00000505975.1:p.His227=
ENST00000680554.1:c.391C= ENSP00000505621.1:p.His131=
ENST00000680576.1:n.468C=
ENST00000680599.1:n.596C=
ENST00000680742.1:c.679C= ENSP00000505206.1:p.His227=
ENST00000680885.1:n.600C=
ENST00000681158.1:c.468C=
ENST00000681173.1:n.468C=
ENST00000681203.1:c.607C= ENSP00000506456.1:p.His203=
ENST00000681425.1:n.600C=
ENST00000681915.1:n.468C=
ENST00000328194.7:c.679C= ENSP00000328524.3:p.His227=
ENST00000526707.5:c.607C= ENSP00000436780.1:p.His203=
ENST00000530044.5:c.679C= ENSP00000435866.1:p.His227=
ENST00000532696.1:n.434C=
NM_001243254.1:c.679C= NP_001230183.1:p.His227=
NM_015213.3:c.679C= NP_056028.2:p.His227=
XM_005252832.1:c.679C= XP_005252889.1:p.His227=
XM_011519952.1:c.679C= XP_011518254.1:p.His227=
XR_242782.2:n.944C=
XR_930851.1:n.944C=
XR_930852.1:n.944C=
XR_930853.1:n.944C=
NM_001348749.1:c.607C= NP_001335678.1:p.His203=
NM_001348750.1:c.391C= NP_001335679.1:p.His131=
NR_145966.2:n.936C=
NM_015213.4:c.679C= MANE Select NP_056028.2:p.His227=
NM_001243254.2:c.679C= NP_001230183.1:p.His227=
NM_001348749.2:c.607C= NP_001335678.1:p.His203=
NM_001348750.2:c.391C= NP_001335679.1:p.His131=