Canonical Allele Identifier: CA379598164

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9142087-T-C
• MyVariant Identifiers: chr11:g.9163634T>C (hg19) ; chr11:g.9142087T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142087T>C , CM000673.2:g.9142087T>C	GRCh38
NC_000011.9:g.9163634T>C , CM000673.1:g.9163634T>C	GRCh37
NC_000011.8:g.9120210T>C	NCBI36
NG_053019.1:g.128249A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3533A>G MANE Select	ENSP00000328524.3:p.Glu1178Gly
ENST00000525784.6:n.1395A>G
ENST00000530780.2:c.*3359A>G	ENSP00000433925.1:n.*3359A>G
ENST00000531747.2:n.3204A>G
ENST00000679446.1:n.3454A>G
ENST00000679458.1:n.4934A>G
ENST00000679460.1:n.4595A>G
ENST00000679568.1:c.3533A>G	ENSP00000505860.1:p.Glu1178Gly
ENST00000679745.1:n.4038A>G
ENST00000679773.1:n.2694A>G
ENST00000679926.1:n.4835A>G
ENST00000679999.1:c.*590A>G	ENSP00000505198.1:n.*590A>G
ENST00000680252.1:c.3200A>G
ENST00000680294.1:c.3326A>G	ENSP00000506113.1:p.Glu1109Gly
ENST00000680358.1:n.2832A>G
ENST00000680470.1:c.*1314A>G	ENSP00000505975.1:n.*1314A>G
ENST00000680554.1:c.*66A>G	ENSP00000505621.1:n.*66A>G
ENST00000680576.1:n.5009A>G
ENST00000680599.1:n.3574A>G
ENST00000680742.1:c.*66A>G	ENSP00000505206.1:n.*66A>G
ENST00000680791.1:n.2417A>G
ENST00000680885.1:n.5235A>G
ENST00000681158.1:c.3117A>G
ENST00000681203.1:c.3461A>G	ENSP00000506456.1:p.Glu1154Gly
ENST00000681371.1:n.3405A>G
ENST00000681425.1:n.4011A>G
ENST00000681639.1:n.1812A>G
ENST00000328194.7:c.3533A>G	ENSP00000328524.3:p.Glu1178Gly
ENST00000525784.5:c.469A>G
ENST00000527700.5:n.3095A>G
ENST00000528725.5:c.229A>G
ENST00000529977.5:n.1434A>G
ENST00000530044.5:c.3533A>G	ENSP00000435866.1:p.Glu1178Gly
ENST00000531747.1:c.769A>G
ENST00000533737.5:c.196A>G
NM_001243254.1:c.3533A>G	NP_001230183.1:p.Glu1178Gly
NM_015213.3:c.3533A>G	NP_056028.2:p.Glu1178Gly
XM_005252832.1:c.3533A>G	XP_005252889.1:p.Glu1178Gly
XM_011519952.1:c.3533A>G	XP_011518254.1:p.Glu1178Gly
XM_011519953.1:c.1631A>G	XP_011518255.1:p.Glu544Gly
XR_242782.2:n.3715A>G
XR_930851.1:n.3715A>G
NM_001348749.1:c.3461A>G	NP_001335678.1:p.Glu1154Gly
NM_001348750.1:c.3245A>G	NP_001335679.1:p.Glu1082Gly
NR_145966.2:n.3707A>G
NM_015213.4:c.3533A>G MANE Select	NP_056028.2:p.Glu1178Gly
NM_001243254.2:c.3533A>G	NP_001230183.1:p.Glu1178Gly
NM_001348749.2:c.3461A>G	NP_001335678.1:p.Glu1154Gly
NM_001348750.2:c.3245A>G	NP_001335679.1:p.Glu1082Gly