Canonical Allele Identifier: CA379597267

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163515A>C (hg19) ; chr11:g.9141968A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141968A>C , CM000673.2:g.9141968A>C	GRCh38
NC_000011.9:g.9163515A>C , CM000673.1:g.9163515A>C	GRCh37
NC_000011.8:g.9120091A>C	NCBI36
NG_053019.1:g.128368T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3652T>G MANE Select	ENSP00000328524.3:p.Phe1218Val
ENST00000525784.6:n.1514T>G
ENST00000530780.2:c.*3478T>G	ENSP00000433925.1:n.*3478T>G
ENST00000531747.2:n.3323T>G
ENST00000679446.1:n.3573T>G
ENST00000679458.1:n.5053T>G
ENST00000679460.1:n.4714T>G
ENST00000679568.1:c.3652T>G	ENSP00000505860.1:p.Phe1218Val
ENST00000679745.1:n.4157T>G
ENST00000679773.1:n.2813T>G
ENST00000679926.1:n.4954T>G
ENST00000679999.1:c.*709T>G	ENSP00000505198.1:n.*709T>G
ENST00000680252.1:c.3319T>G
ENST00000680294.1:c.3445T>G	ENSP00000506113.1:p.Phe1149Val
ENST00000680358.1:n.2951T>G
ENST00000680470.1:c.*1433T>G	ENSP00000505975.1:n.*1433T>G
ENST00000680554.1:c.*185T>G	ENSP00000505621.1:n.*185T>G
ENST00000680576.1:n.5128T>G
ENST00000680599.1:n.3693T>G
ENST00000680742.1:c.*179+6T>G	ENSP00000505206.1:n.*179+6T>G
ENST00000680791.1:n.2536T>G
ENST00000680885.1:n.5354T>G
ENST00000681158.1:c.3236T>G
ENST00000681203.1:c.3580T>G	ENSP00000506456.1:p.Phe1194Val
ENST00000681371.1:n.3524T>G
ENST00000681425.1:n.4130T>G
ENST00000681639.1:n.1931T>G
ENST00000328194.7:c.3652T>G	ENSP00000328524.3:p.Phe1218Val
ENST00000525784.5:c.588T>G
ENST00000527700.5:n.3214T>G
ENST00000528725.5:c.348T>G
ENST00000529977.5:n.1553T>G
ENST00000530044.5:c.3646+6T>G	ENSP00000435866.1:n.3646+6T>G
ENST00000531747.1:c.888T>G
ENST00000533737.5:c.315T>G
NM_001243254.1:c.3646+6T>G	NP_001230183.1:n.3646+6T>G
NM_015213.3:c.3652T>G	NP_056028.2:p.Phe1218Val
XM_005252832.1:c.3652T>G	XP_005252889.1:p.Phe1218Val
XM_011519952.1:c.3646+6T>G	XP_011518254.1:n.3646+6T>G
XM_011519953.1:c.1750T>G	XP_011518255.1:p.Phe584Val
XR_242782.2:n.3834T>G
XR_930851.1:n.3828+6T>G
NM_001348749.1:c.3580T>G	NP_001335678.1:p.Phe1194Val
NM_001348750.1:c.3364T>G	NP_001335679.1:p.Phe1122Val
NR_145966.2:n.3826T>G
NM_015213.4:c.3652T>G MANE Select	NP_056028.2:p.Phe1218Val
NM_001243254.2:c.3646+6T>G	NP_001230183.1:n.3646+6T>G
NM_001348749.2:c.3580T>G	NP_001335678.1:p.Phe1194Val
NM_001348750.2:c.3364T>G	NP_001335679.1:p.Phe1122Val