Canonical Allele Identifier: CA473040220

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163555T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142008T>C , CM000673.2:g.9142008T>C	GRCh38
NC_000011.9:g.9163555T>C , CM000673.1:g.9163555T>C	GRCh37
NC_000011.8:g.9120131T>C	NCBI36
NG_053019.1:g.128328A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3612A>G MANE Select	ENSP00000328524.3:p.Ala1204=
ENST00000525784.6:n.1474A>G
ENST00000530780.2:c.*3438A>G	ENSP00000433925.1:n.*3438A>G
ENST00000531747.2:n.3283A>G
ENST00000679446.1:n.3533A>G
ENST00000679458.1:n.5013A>G
ENST00000679460.1:n.4674A>G
ENST00000679568.1:c.3612A>G	ENSP00000505860.1:p.Ala1204=
ENST00000679745.1:n.4117A>G
ENST00000679773.1:n.2773A>G
ENST00000679926.1:n.4914A>G
ENST00000679999.1:c.*669A>G	ENSP00000505198.1:n.*669A>G
ENST00000680252.1:c.3279A>G
ENST00000680294.1:c.3405A>G	ENSP00000506113.1:p.Ala1135=
ENST00000680358.1:n.2911A>G
ENST00000680470.1:c.*1393A>G	ENSP00000505975.1:n.*1393A>G
ENST00000680554.1:c.*145A>G	ENSP00000505621.1:n.*145A>G
ENST00000680576.1:n.5088A>G
ENST00000680599.1:n.3653A>G
ENST00000680742.1:c.*145A>G	ENSP00000505206.1:n.*145A>G
ENST00000680791.1:n.2496A>G
ENST00000680885.1:n.5314A>G
ENST00000681158.1:c.3196A>G
ENST00000681203.1:c.3540A>G	ENSP00000506456.1:p.Ala1180=
ENST00000681371.1:n.3484A>G
ENST00000681425.1:n.4090A>G
ENST00000681639.1:n.1891A>G
ENST00000328194.7:c.3612A>G	ENSP00000328524.3:p.Ala1204=
ENST00000525784.5:c.548A>G
ENST00000527700.5:n.3174A>G
ENST00000528725.5:c.308A>G
ENST00000529977.5:n.1513A>G
ENST00000530044.5:c.3612A>G	ENSP00000435866.1:p.Ala1204=
ENST00000531747.1:c.848A>G
ENST00000533737.5:c.275A>G
NM_001243254.1:c.3612A>G	NP_001230183.1:p.Ala1204=
NM_015213.3:c.3612A>G	NP_056028.2:p.Ala1204=
XM_005252832.1:c.3612A>G	XP_005252889.1:p.Ala1204=
XM_011519952.1:c.3612A>G	XP_011518254.1:p.Ala1204=
XM_011519953.1:c.1710A>G	XP_011518255.1:p.Ala570=
XR_242782.2:n.3794A>G
XR_930851.1:n.3794A>G
NM_001348749.1:c.3540A>G	NP_001335678.1:p.Ala1180=
NM_001348750.1:c.3324A>G	NP_001335679.1:p.Ala1108=
NR_145966.2:n.3786A>G
NM_015213.4:c.3612A>G MANE Select	NP_056028.2:p.Ala1204=
NM_001243254.2:c.3612A>G	NP_001230183.1:p.Ala1204=
NM_001348749.2:c.3540A>G	NP_001335678.1:p.Ala1180=
NM_001348750.2:c.3324A>G	NP_001335679.1:p.Ala1108=