Canonical Allele Identifier: CA379597389

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163529C>T (hg19) ; chr11:g.9141982C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141982C>T , CM000673.2:g.9141982C>T	GRCh38
NC_000011.9:g.9163529C>T , CM000673.1:g.9163529C>T	GRCh37
NC_000011.8:g.9120105C>T	NCBI36
NG_053019.1:g.128354G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3638G>A MANE Select	ENSP00000328524.3:p.Gly1213Asp
ENST00000525784.6:n.1500G>A
ENST00000530780.2:c.*3464G>A	ENSP00000433925.1:n.*3464G>A
ENST00000531747.2:n.3309G>A
ENST00000679446.1:n.3559G>A
ENST00000679458.1:n.5039G>A
ENST00000679460.1:n.4700G>A
ENST00000679568.1:c.3638G>A	ENSP00000505860.1:p.Gly1213Asp
ENST00000679745.1:n.4143G>A
ENST00000679773.1:n.2799G>A
ENST00000679926.1:n.4940G>A
ENST00000679999.1:c.*695G>A	ENSP00000505198.1:n.*695G>A
ENST00000680252.1:c.3305G>A
ENST00000680294.1:c.3431G>A	ENSP00000506113.1:p.Gly1144Asp
ENST00000680358.1:n.2937G>A
ENST00000680470.1:c.*1419G>A	ENSP00000505975.1:n.*1419G>A
ENST00000680554.1:c.*171G>A	ENSP00000505621.1:n.*171G>A
ENST00000680576.1:n.5114G>A
ENST00000680599.1:n.3679G>A
ENST00000680742.1:c.*171G>A	ENSP00000505206.1:n.*171G>A
ENST00000680791.1:n.2522G>A
ENST00000680885.1:n.5340G>A
ENST00000681158.1:c.3222G>A
ENST00000681203.1:c.3566G>A	ENSP00000506456.1:p.Gly1189Asp
ENST00000681371.1:n.3510G>A
ENST00000681425.1:n.4116G>A
ENST00000681639.1:n.1917G>A
ENST00000328194.7:c.3638G>A	ENSP00000328524.3:p.Gly1213Asp
ENST00000525784.5:c.574G>A
ENST00000527700.5:n.3200G>A
ENST00000528725.5:c.334G>A
ENST00000529977.5:n.1539G>A
ENST00000530044.5:c.3638G>A	ENSP00000435866.1:p.Gly1213Asp
ENST00000531747.1:c.874G>A
ENST00000533737.5:c.301G>A
NM_001243254.1:c.3638G>A	NP_001230183.1:p.Gly1213Asp
NM_015213.3:c.3638G>A	NP_056028.2:p.Gly1213Asp
XM_005252832.1:c.3638G>A	XP_005252889.1:p.Gly1213Asp
XM_011519952.1:c.3638G>A	XP_011518254.1:p.Gly1213Asp
XM_011519953.1:c.1736G>A	XP_011518255.1:p.Gly579Asp
XR_242782.2:n.3820G>A
XR_930851.1:n.3820G>A
NM_001348749.1:c.3566G>A	NP_001335678.1:p.Gly1189Asp
NM_001348750.1:c.3350G>A	NP_001335679.1:p.Gly1117Asp
NR_145966.2:n.3812G>A
NM_015213.4:c.3638G>A MANE Select	NP_056028.2:p.Gly1213Asp
NM_001243254.2:c.3638G>A	NP_001230183.1:p.Gly1213Asp
NM_001348749.2:c.3566G>A	NP_001335678.1:p.Gly1189Asp
NM_001348750.2:c.3350G>A	NP_001335679.1:p.Gly1117Asp