Canonical Allele Identifier: CA379598174

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163635C>T (hg19) ; chr11:g.9142088C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142088C>T , CM000673.2:g.9142088C>T	GRCh38
NC_000011.9:g.9163635C>T , CM000673.1:g.9163635C>T	GRCh37
NC_000011.8:g.9120211C>T	NCBI36
NG_053019.1:g.128248G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3532G>A MANE Select	ENSP00000328524.3:p.Glu1178Lys
ENST00000525784.6:n.1394G>A
ENST00000530780.2:c.*3358G>A	ENSP00000433925.1:n.*3358G>A
ENST00000531747.2:n.3203G>A
ENST00000679446.1:n.3453G>A
ENST00000679458.1:n.4933G>A
ENST00000679460.1:n.4594G>A
ENST00000679568.1:c.3532G>A	ENSP00000505860.1:p.Glu1178Lys
ENST00000679745.1:n.4037G>A
ENST00000679773.1:n.2693G>A
ENST00000679926.1:n.4834G>A
ENST00000679999.1:c.*589G>A	ENSP00000505198.1:n.*589G>A
ENST00000680252.1:c.3199G>A
ENST00000680294.1:c.3325G>A	ENSP00000506113.1:p.Glu1109Lys
ENST00000680358.1:n.2831G>A
ENST00000680470.1:c.*1313G>A	ENSP00000505975.1:n.*1313G>A
ENST00000680554.1:c.*65G>A	ENSP00000505621.1:n.*65G>A
ENST00000680576.1:n.5008G>A
ENST00000680599.1:n.3573G>A
ENST00000680742.1:c.*65G>A	ENSP00000505206.1:n.*65G>A
ENST00000680791.1:n.2416G>A
ENST00000680885.1:n.5234G>A
ENST00000681158.1:c.3116G>A
ENST00000681203.1:c.3460G>A	ENSP00000506456.1:p.Glu1154Lys
ENST00000681371.1:n.3404G>A
ENST00000681425.1:n.4010G>A
ENST00000681639.1:n.1811G>A
ENST00000328194.7:c.3532G>A	ENSP00000328524.3:p.Glu1178Lys
ENST00000525784.5:c.468G>A
ENST00000527700.5:n.3094G>A
ENST00000528725.5:c.228G>A
ENST00000529977.5:n.1433G>A
ENST00000530044.5:c.3532G>A	ENSP00000435866.1:p.Glu1178Lys
ENST00000531747.1:c.768G>A
ENST00000533737.5:c.195G>A
NM_001243254.1:c.3532G>A	NP_001230183.1:p.Glu1178Lys
NM_015213.3:c.3532G>A	NP_056028.2:p.Glu1178Lys
XM_005252832.1:c.3532G>A	XP_005252889.1:p.Glu1178Lys
XM_011519952.1:c.3532G>A	XP_011518254.1:p.Glu1178Lys
XM_011519953.1:c.1630G>A	XP_011518255.1:p.Glu544Lys
XR_242782.2:n.3714G>A
XR_930851.1:n.3714G>A
NM_001348749.1:c.3460G>A	NP_001335678.1:p.Glu1154Lys
NM_001348750.1:c.3244G>A	NP_001335679.1:p.Glu1082Lys
NR_145966.2:n.3706G>A
NM_015213.4:c.3532G>A MANE Select	NP_056028.2:p.Glu1178Lys
NM_001243254.2:c.3532G>A	NP_001230183.1:p.Glu1178Lys
NM_001348749.2:c.3460G>A	NP_001335678.1:p.Glu1154Lys
NM_001348750.2:c.3244G>A	NP_001335679.1:p.Glu1082Lys