Canonical Allele Identifier: CA379598255

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163650C>A (hg19) ; chr11:g.9142103C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142103C>A , CM000673.2:g.9142103C>A	GRCh38
NC_000011.9:g.9163650C>A , CM000673.1:g.9163650C>A	GRCh37
NC_000011.8:g.9120226C>A	NCBI36
NG_053019.1:g.128233G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3517G>T MANE Select	ENSP00000328524.3:p.Ala1173Ser
ENST00000525784.6:n.1379G>T
ENST00000530780.2:c.*3343G>T	ENSP00000433925.1:n.*3343G>T
ENST00000531747.2:n.3188G>T
ENST00000679446.1:n.3438G>T
ENST00000679458.1:n.4918G>T
ENST00000679460.1:n.4579G>T
ENST00000679568.1:c.3517G>T	ENSP00000505860.1:p.Ala1173Ser
ENST00000679745.1:n.4022G>T
ENST00000679773.1:n.2678G>T
ENST00000679926.1:n.4819G>T
ENST00000679999.1:c.*574G>T	ENSP00000505198.1:n.*574G>T
ENST00000680252.1:c.3184G>T
ENST00000680294.1:c.3310G>T	ENSP00000506113.1:p.Ala1104Ser
ENST00000680358.1:n.2816G>T
ENST00000680470.1:c.*1298G>T	ENSP00000505975.1:n.*1298G>T
ENST00000680554.1:c.*50G>T	ENSP00000505621.1:n.*50G>T
ENST00000680576.1:n.4993G>T
ENST00000680599.1:n.3558G>T
ENST00000680742.1:c.*50G>T	ENSP00000505206.1:n.*50G>T
ENST00000680791.1:n.2401G>T
ENST00000680885.1:n.5219G>T
ENST00000681158.1:c.3101G>T
ENST00000681203.1:c.3445G>T	ENSP00000506456.1:p.Ala1149Ser
ENST00000681371.1:n.3389G>T
ENST00000681425.1:n.3995G>T
ENST00000681639.1:n.1796G>T
ENST00000328194.7:c.3517G>T	ENSP00000328524.3:p.Ala1173Ser
ENST00000525784.5:c.453G>T
ENST00000527700.5:n.3079G>T
ENST00000528725.5:c.213G>T
ENST00000529977.5:n.1418G>T
ENST00000530044.5:c.3517G>T	ENSP00000435866.1:p.Ala1173Ser
ENST00000531747.1:c.753G>T
ENST00000533737.5:c.180G>T
NM_001243254.1:c.3517G>T	NP_001230183.1:p.Ala1173Ser
NM_015213.3:c.3517G>T	NP_056028.2:p.Ala1173Ser
XM_005252832.1:c.3517G>T	XP_005252889.1:p.Ala1173Ser
XM_011519952.1:c.3517G>T	XP_011518254.1:p.Ala1173Ser
XM_011519953.1:c.1615G>T	XP_011518255.1:p.Ala539Ser
XR_242782.2:n.3699G>T
XR_930851.1:n.3699G>T
NM_001348749.1:c.3445G>T	NP_001335678.1:p.Ala1149Ser
NM_001348750.1:c.3229G>T	NP_001335679.1:p.Ala1077Ser
NR_145966.2:n.3691G>T
NM_015213.4:c.3517G>T MANE Select	NP_056028.2:p.Ala1173Ser
NM_001243254.2:c.3517G>T	NP_001230183.1:p.Ala1173Ser
NM_001348749.2:c.3445G>T	NP_001335678.1:p.Ala1149Ser
NM_001348750.2:c.3229G>T	NP_001335679.1:p.Ala1077Ser