Canonical Allele Identifier: CA379598056

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163615T>A (hg19) ; chr11:g.9142068T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142068T>A , CM000673.2:g.9142068T>A	GRCh38
NC_000011.9:g.9163615T>A , CM000673.1:g.9163615T>A	GRCh37
NC_000011.8:g.9120191T>A	NCBI36
NG_053019.1:g.128268A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3552A>T MANE Select	ENSP00000328524.3:p.Glu1184Asp
ENST00000525784.6:n.1414A>T
ENST00000530780.2:c.*3378A>T	ENSP00000433925.1:n.*3378A>T
ENST00000531747.2:n.3223A>T
ENST00000679446.1:n.3473A>T
ENST00000679458.1:n.4953A>T
ENST00000679460.1:n.4614A>T
ENST00000679568.1:c.3552A>T	ENSP00000505860.1:p.Glu1184Asp
ENST00000679745.1:n.4057A>T
ENST00000679773.1:n.2713A>T
ENST00000679926.1:n.4854A>T
ENST00000679999.1:c.*609A>T	ENSP00000505198.1:n.*609A>T
ENST00000680252.1:c.3219A>T
ENST00000680294.1:c.3345A>T	ENSP00000506113.1:p.Glu1115Asp
ENST00000680358.1:n.2851A>T
ENST00000680470.1:c.*1333A>T	ENSP00000505975.1:n.*1333A>T
ENST00000680554.1:c.*85A>T	ENSP00000505621.1:n.*85A>T
ENST00000680576.1:n.5028A>T
ENST00000680599.1:n.3593A>T
ENST00000680742.1:c.*85A>T	ENSP00000505206.1:n.*85A>T
ENST00000680791.1:n.2436A>T
ENST00000680885.1:n.5254A>T
ENST00000681158.1:c.3136A>T
ENST00000681203.1:c.3480A>T	ENSP00000506456.1:p.Glu1160Asp
ENST00000681371.1:n.3424A>T
ENST00000681425.1:n.4030A>T
ENST00000681639.1:n.1831A>T
ENST00000328194.7:c.3552A>T	ENSP00000328524.3:p.Glu1184Asp
ENST00000525784.5:c.488A>T
ENST00000527700.5:n.3114A>T
ENST00000528725.5:c.248A>T
ENST00000529977.5:n.1453A>T
ENST00000530044.5:c.3552A>T	ENSP00000435866.1:p.Glu1184Asp
ENST00000531747.1:c.788A>T
ENST00000533737.5:c.215A>T
NM_001243254.1:c.3552A>T	NP_001230183.1:p.Glu1184Asp
NM_015213.3:c.3552A>T	NP_056028.2:p.Glu1184Asp
XM_005252832.1:c.3552A>T	XP_005252889.1:p.Glu1184Asp
XM_011519952.1:c.3552A>T	XP_011518254.1:p.Glu1184Asp
XM_011519953.1:c.1650A>T	XP_011518255.1:p.Glu550Asp
XR_242782.2:n.3734A>T
XR_930851.1:n.3734A>T
NM_001348749.1:c.3480A>T	NP_001335678.1:p.Glu1160Asp
NM_001348750.1:c.3264A>T	NP_001335679.1:p.Glu1088Asp
NR_145966.2:n.3726A>T
NM_015213.4:c.3552A>T MANE Select	NP_056028.2:p.Glu1184Asp
NM_001243254.2:c.3552A>T	NP_001230183.1:p.Glu1184Asp
NM_001348749.2:c.3480A>T	NP_001335678.1:p.Glu1160Asp
NM_001348750.2:c.3264A>T	NP_001335679.1:p.Glu1088Asp