Canonical Allele Identifier: CA379597158

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163500A>C (hg19) ; chr11:g.9141953A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141953A>C , CM000673.2:g.9141953A>C	GRCh38
NC_000011.9:g.9163500A>C , CM000673.1:g.9163500A>C	GRCh37
NC_000011.8:g.9120076A>C	NCBI36
NG_053019.1:g.128383T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3667T>G MANE Select	ENSP00000328524.3:p.Cys1223Gly
ENST00000525784.6:n.1529T>G
ENST00000530780.2:c.*3493T>G	ENSP00000433925.1:n.*3493T>G
ENST00000531747.2:n.3338T>G
ENST00000679446.1:n.3588T>G
ENST00000679458.1:n.5068T>G
ENST00000679460.1:n.4729T>G
ENST00000679568.1:c.3667T>G	ENSP00000505860.1:p.Cys1223Gly
ENST00000679745.1:n.4172T>G
ENST00000679773.1:n.2828T>G
ENST00000679926.1:n.4969T>G
ENST00000679999.1:c.*724T>G	ENSP00000505198.1:n.*724T>G
ENST00000680252.1:c.3334T>G
ENST00000680294.1:c.3460T>G	ENSP00000506113.1:p.Cys1154Gly
ENST00000680358.1:n.2966T>G
ENST00000680470.1:c.*1448T>G	ENSP00000505975.1:n.*1448T>G
ENST00000680554.1:c.*200T>G	ENSP00000505621.1:n.*200T>G
ENST00000680576.1:n.5143T>G
ENST00000680599.1:n.3708T>G
ENST00000680742.1:c.*179+21T>G	ENSP00000505206.1:n.*179+21T>G
ENST00000680791.1:n.2551T>G
ENST00000680885.1:n.5369T>G
ENST00000681158.1:c.3251T>G
ENST00000681203.1:c.3595T>G	ENSP00000506456.1:p.Cys1199Gly
ENST00000681371.1:n.3539T>G
ENST00000681425.1:n.4145T>G
ENST00000681639.1:n.1946T>G
ENST00000328194.7:c.3667T>G	ENSP00000328524.3:p.Cys1223Gly
ENST00000525784.5:c.603T>G
ENST00000527700.5:n.3229T>G
ENST00000528725.5:c.363T>G
ENST00000529977.5:n.1568T>G
ENST00000530044.5:c.3646+21T>G	ENSP00000435866.1:n.3646+21T>G
ENST00000531747.1:c.903T>G
ENST00000533737.5:c.330T>G
NM_001243254.1:c.3646+21T>G	NP_001230183.1:n.3646+21T>G
NM_015213.3:c.3667T>G	NP_056028.2:p.Cys1223Gly
XM_005252832.1:c.3667T>G	XP_005252889.1:p.Cys1223Gly
XM_011519952.1:c.3646+21T>G	XP_011518254.1:n.3646+21T>G
XM_011519953.1:c.1765T>G	XP_011518255.1:p.Cys589Gly
XR_242782.2:n.3849T>G
XR_930851.1:n.3828+21T>G
NM_001348749.1:c.3595T>G	NP_001335678.1:p.Cys1199Gly
NM_001348750.1:c.3379T>G	NP_001335679.1:p.Cys1127Gly
NR_145966.2:n.3841T>G
NM_015213.4:c.3667T>G MANE Select	NP_056028.2:p.Cys1223Gly
NM_001243254.2:c.3646+21T>G	NP_001230183.1:n.3646+21T>G
NM_001348749.2:c.3595T>G	NP_001335678.1:p.Cys1199Gly
NM_001348750.2:c.3379T>G	NP_001335679.1:p.Cys1127Gly