Canonical Allele Identifier: CA379598860
Gene: DENND5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9203986C>A , CM000673.2:g.9203986C>A GRCh38
NC_000011.9:g.9225533C>A , CM000673.1:g.9225533C>A GRCh37
NC_000011.8:g.9182109C>A NCBI36
NG_053019.1:g.66350G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.623G>T MANE Select ENSP00000328524.3:p.Cys208Phe
ENST00000530780.2:c.*449G>T ENSP00000433925.1:n.*449G>T
ENST00000530867.2:n.412G>T
ENST00000532696.2:n.546G>T
ENST00000679446.1:n.544G>T
ENST00000679460.1:n.412G>T
ENST00000679568.1:c.623G>T ENSP00000505860.1:p.Cys208Phe
ENST00000679745.1:n.412G>T
ENST00000679999.1:c.623G>T ENSP00000505198.1:p.Cys208Phe
ENST00000680252.1:c.412G>T
ENST00000680294.1:c.623G>T ENSP00000506113.1:p.Cys208Phe
ENST00000680470.1:c.623G>T ENSP00000505975.1:p.Cys208Phe
ENST00000680554.1:c.335G>T ENSP00000505621.1:p.Cys112Phe
ENST00000680576.1:n.412G>T
ENST00000680599.1:n.540G>T
ENST00000680742.1:c.623G>T ENSP00000505206.1:p.Cys208Phe
ENST00000680885.1:n.544G>T
ENST00000681158.1:c.412G>T
ENST00000681173.1:n.412G>T
ENST00000681203.1:c.551G>T ENSP00000506456.1:p.Cys184Phe
ENST00000681425.1:n.544G>T
ENST00000681915.1:n.412G>T
ENST00000328194.7:c.623G>T ENSP00000328524.3:p.Cys208Phe
ENST00000526707.5:c.551G>T ENSP00000436780.1:p.Cys184Phe
ENST00000530044.5:c.623G>T ENSP00000435866.1:p.Cys208Phe
ENST00000532696.1:n.378G>T
NM_001243254.1:c.623G>T NP_001230183.1:p.Cys208Phe
NM_015213.3:c.623G>T NP_056028.2:p.Cys208Phe
XM_005252832.1:c.623G>T XP_005252889.1:p.Cys208Phe
XM_011519952.1:c.623G>T XP_011518254.1:p.Cys208Phe
XR_242782.2:n.888G>T
XR_930851.1:n.888G>T
XR_930852.1:n.888G>T
XR_930853.1:n.888G>T
NM_001348749.1:c.551G>T NP_001335678.1:p.Cys184Phe
NM_001348750.1:c.335G>T NP_001335679.1:p.Cys112Phe
NR_145966.2:n.880G>T
NM_015213.4:c.623G>T MANE Select NP_056028.2:p.Cys208Phe
NM_001243254.2:c.623G>T NP_001230183.1:p.Cys208Phe
NM_001348749.2:c.551G>T NP_001335678.1:p.Cys184Phe
NM_001348750.2:c.335G>T NP_001335679.1:p.Cys112Phe