Canonical Allele Identifier: CA379598107

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163624C>G (hg19) ; chr11:g.9142077C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142077C>G , CM000673.2:g.9142077C>G	GRCh38
NC_000011.9:g.9163624C>G , CM000673.1:g.9163624C>G	GRCh37
NC_000011.8:g.9120200C>G	NCBI36
NG_053019.1:g.128259G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3543G>C MANE Select	ENSP00000328524.3:p.Glu1181Asp
ENST00000525784.6:n.1405G>C
ENST00000530780.2:c.*3369G>C	ENSP00000433925.1:n.*3369G>C
ENST00000531747.2:n.3214G>C
ENST00000679446.1:n.3464G>C
ENST00000679458.1:n.4944G>C
ENST00000679460.1:n.4605G>C
ENST00000679568.1:c.3543G>C	ENSP00000505860.1:p.Glu1181Asp
ENST00000679745.1:n.4048G>C
ENST00000679773.1:n.2704G>C
ENST00000679926.1:n.4845G>C
ENST00000679999.1:c.*600G>C	ENSP00000505198.1:n.*600G>C
ENST00000680252.1:c.3210G>C
ENST00000680294.1:c.3336G>C	ENSP00000506113.1:p.Glu1112Asp
ENST00000680358.1:n.2842G>C
ENST00000680470.1:c.*1324G>C	ENSP00000505975.1:n.*1324G>C
ENST00000680554.1:c.*76G>C	ENSP00000505621.1:n.*76G>C
ENST00000680576.1:n.5019G>C
ENST00000680599.1:n.3584G>C
ENST00000680742.1:c.*76G>C	ENSP00000505206.1:n.*76G>C
ENST00000680791.1:n.2427G>C
ENST00000680885.1:n.5245G>C
ENST00000681158.1:c.3127G>C
ENST00000681203.1:c.3471G>C	ENSP00000506456.1:p.Glu1157Asp
ENST00000681371.1:n.3415G>C
ENST00000681425.1:n.4021G>C
ENST00000681639.1:n.1822G>C
ENST00000328194.7:c.3543G>C	ENSP00000328524.3:p.Glu1181Asp
ENST00000525784.5:c.479G>C
ENST00000527700.5:n.3105G>C
ENST00000528725.5:c.239G>C
ENST00000529977.5:n.1444G>C
ENST00000530044.5:c.3543G>C	ENSP00000435866.1:p.Glu1181Asp
ENST00000531747.1:c.779G>C
ENST00000533737.5:c.206G>C
NM_001243254.1:c.3543G>C	NP_001230183.1:p.Glu1181Asp
NM_015213.3:c.3543G>C	NP_056028.2:p.Glu1181Asp
XM_005252832.1:c.3543G>C	XP_005252889.1:p.Glu1181Asp
XM_011519952.1:c.3543G>C	XP_011518254.1:p.Glu1181Asp
XM_011519953.1:c.1641G>C	XP_011518255.1:p.Glu547Asp
XR_242782.2:n.3725G>C
XR_930851.1:n.3725G>C
NM_001348749.1:c.3471G>C	NP_001335678.1:p.Glu1157Asp
NM_001348750.1:c.3255G>C	NP_001335679.1:p.Glu1085Asp
NR_145966.2:n.3717G>C
NM_015213.4:c.3543G>C MANE Select	NP_056028.2:p.Glu1181Asp
NM_001243254.2:c.3543G>C	NP_001230183.1:p.Glu1181Asp
NM_001348749.2:c.3471G>C	NP_001335678.1:p.Glu1157Asp
NM_001348750.2:c.3255G>C	NP_001335679.1:p.Glu1085Asp