Canonical Allele Identifier: CA473040179

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163488T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141941T>G , CM000673.2:g.9141941T>G	GRCh38
NC_000011.9:g.9163488T>G , CM000673.1:g.9163488T>G	GRCh37
NC_000011.8:g.9120064T>G	NCBI36
NG_053019.1:g.128395A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3679A>C MANE Select	ENSP00000328524.3:p.Arg1227=
ENST00000525784.6:n.1541A>C
ENST00000530780.2:c.*3505A>C	ENSP00000433925.1:n.*3505A>C
ENST00000531747.2:n.3350A>C
ENST00000679446.1:n.3600A>C
ENST00000679458.1:n.5080A>C
ENST00000679460.1:n.4741A>C
ENST00000679568.1:c.3679A>C	ENSP00000505860.1:p.Arg1227=
ENST00000679745.1:n.4184A>C
ENST00000679773.1:n.2840A>C
ENST00000679926.1:n.4981A>C
ENST00000679999.1:c.*736A>C	ENSP00000505198.1:n.*736A>C
ENST00000680252.1:c.3346A>C
ENST00000680294.1:c.3472A>C	ENSP00000506113.1:p.Arg1158=
ENST00000680358.1:n.2978A>C
ENST00000680470.1:c.*1460A>C	ENSP00000505975.1:n.*1460A>C
ENST00000680554.1:c.*212A>C	ENSP00000505621.1:n.*212A>C
ENST00000680576.1:n.5155A>C
ENST00000680599.1:n.3720A>C
ENST00000680742.1:c.*179+33A>C	ENSP00000505206.1:n.*179+33A>C
ENST00000680791.1:n.2563A>C
ENST00000680885.1:n.5381A>C
ENST00000681158.1:c.3263A>C
ENST00000681203.1:c.3607A>C	ENSP00000506456.1:p.Arg1203=
ENST00000681371.1:n.3551A>C
ENST00000681425.1:n.4157A>C
ENST00000681639.1:n.1958A>C
ENST00000328194.7:c.3679A>C	ENSP00000328524.3:p.Arg1227=
ENST00000525784.5:c.615A>C
ENST00000527700.5:n.3241A>C
ENST00000528725.5:c.375A>C
ENST00000529977.5:n.1580A>C
ENST00000530044.5:c.3646+33A>C	ENSP00000435866.1:n.3646+33A>C
ENST00000531747.1:c.915A>C
ENST00000533737.5:c.342A>C
NM_001243254.1:c.3646+33A>C	NP_001230183.1:n.3646+33A>C
NM_015213.3:c.3679A>C	NP_056028.2:p.Arg1227=
XM_005252832.1:c.3679A>C	XP_005252889.1:p.Arg1227=
XM_011519952.1:c.3646+33A>C	XP_011518254.1:n.3646+33A>C
XM_011519953.1:c.1777A>C	XP_011518255.1:p.Arg593=
XR_242782.2:n.3861A>C
XR_930851.1:n.3828+33A>C
NM_001348749.1:c.3607A>C	NP_001335678.1:p.Arg1203=
NM_001348750.1:c.3391A>C	NP_001335679.1:p.Arg1131=
NR_145966.2:n.3853A>C
NM_015213.4:c.3679A>C MANE Select	NP_056028.2:p.Arg1227=
NM_001243254.2:c.3646+33A>C	NP_001230183.1:n.3646+33A>C
NM_001348749.2:c.3607A>C	NP_001335678.1:p.Arg1203=
NM_001348750.2:c.3391A>C	NP_001335679.1:p.Arg1131=