Canonical Allele Identifier: CA379598134

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163629A>C (hg19) ; chr11:g.9142082A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142082A>C , CM000673.2:g.9142082A>C	GRCh38
NC_000011.9:g.9163629A>C , CM000673.1:g.9163629A>C	GRCh37
NC_000011.8:g.9120205A>C	NCBI36
NG_053019.1:g.128254T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3538T>G MANE Select	ENSP00000328524.3:p.Leu1180Val
ENST00000525784.6:n.1400T>G
ENST00000530780.2:c.*3364T>G	ENSP00000433925.1:n.*3364T>G
ENST00000531747.2:n.3209T>G
ENST00000679446.1:n.3459T>G
ENST00000679458.1:n.4939T>G
ENST00000679460.1:n.4600T>G
ENST00000679568.1:c.3538T>G	ENSP00000505860.1:p.Leu1180Val
ENST00000679745.1:n.4043T>G
ENST00000679773.1:n.2699T>G
ENST00000679926.1:n.4840T>G
ENST00000679999.1:c.*595T>G	ENSP00000505198.1:n.*595T>G
ENST00000680252.1:c.3205T>G
ENST00000680294.1:c.3331T>G	ENSP00000506113.1:p.Leu1111Val
ENST00000680358.1:n.2837T>G
ENST00000680470.1:c.*1319T>G	ENSP00000505975.1:n.*1319T>G
ENST00000680554.1:c.*71T>G	ENSP00000505621.1:n.*71T>G
ENST00000680576.1:n.5014T>G
ENST00000680599.1:n.3579T>G
ENST00000680742.1:c.*71T>G	ENSP00000505206.1:n.*71T>G
ENST00000680791.1:n.2422T>G
ENST00000680885.1:n.5240T>G
ENST00000681158.1:c.3122T>G
ENST00000681203.1:c.3466T>G	ENSP00000506456.1:p.Leu1156Val
ENST00000681371.1:n.3410T>G
ENST00000681425.1:n.4016T>G
ENST00000681639.1:n.1817T>G
ENST00000328194.7:c.3538T>G	ENSP00000328524.3:p.Leu1180Val
ENST00000525784.5:c.474T>G
ENST00000527700.5:n.3100T>G
ENST00000528725.5:c.234T>G
ENST00000529977.5:n.1439T>G
ENST00000530044.5:c.3538T>G	ENSP00000435866.1:p.Leu1180Val
ENST00000531747.1:c.774T>G
ENST00000533737.5:c.201T>G
NM_001243254.1:c.3538T>G	NP_001230183.1:p.Leu1180Val
NM_015213.3:c.3538T>G	NP_056028.2:p.Leu1180Val
XM_005252832.1:c.3538T>G	XP_005252889.1:p.Leu1180Val
XM_011519952.1:c.3538T>G	XP_011518254.1:p.Leu1180Val
XM_011519953.1:c.1636T>G	XP_011518255.1:p.Leu546Val
XR_242782.2:n.3720T>G
XR_930851.1:n.3720T>G
NM_001348749.1:c.3466T>G	NP_001335678.1:p.Leu1156Val
NM_001348750.1:c.3250T>G	NP_001335679.1:p.Leu1084Val
NR_145966.2:n.3712T>G
NM_015213.4:c.3538T>G MANE Select	NP_056028.2:p.Leu1180Val
NM_001243254.2:c.3538T>G	NP_001230183.1:p.Leu1180Val
NM_001348749.2:c.3466T>G	NP_001335678.1:p.Leu1156Val
NM_001348750.2:c.3250T>G	NP_001335679.1:p.Leu1084Val