Canonical Allele Identifier: CA473040200

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163522A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141975A>G , CM000673.2:g.9141975A>G	GRCh38
NC_000011.9:g.9163522A>G , CM000673.1:g.9163522A>G	GRCh37
NC_000011.8:g.9120098A>G	NCBI36
NG_053019.1:g.128361T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3645T>C MANE Select	ENSP00000328524.3:p.Asp1215=
ENST00000525784.6:n.1507T>C
ENST00000530780.2:c.*3471T>C	ENSP00000433925.1:n.*3471T>C
ENST00000531747.2:n.3316T>C
ENST00000679446.1:n.3566T>C
ENST00000679458.1:n.5046T>C
ENST00000679460.1:n.4707T>C
ENST00000679568.1:c.3645T>C	ENSP00000505860.1:p.Asp1215=
ENST00000679745.1:n.4150T>C
ENST00000679773.1:n.2806T>C
ENST00000679926.1:n.4947T>C
ENST00000679999.1:c.*702T>C	ENSP00000505198.1:n.*702T>C
ENST00000680252.1:c.3312T>C
ENST00000680294.1:c.3438T>C	ENSP00000506113.1:p.Asp1146=
ENST00000680358.1:n.2944T>C
ENST00000680470.1:c.*1426T>C	ENSP00000505975.1:n.*1426T>C
ENST00000680554.1:c.*178T>C	ENSP00000505621.1:n.*178T>C
ENST00000680576.1:n.5121T>C
ENST00000680599.1:n.3686T>C
ENST00000680742.1:c.*178T>C	ENSP00000505206.1:n.*178T>C
ENST00000680791.1:n.2529T>C
ENST00000680885.1:n.5347T>C
ENST00000681158.1:c.3229T>C
ENST00000681203.1:c.3573T>C	ENSP00000506456.1:p.Asp1191=
ENST00000681371.1:n.3517T>C
ENST00000681425.1:n.4123T>C
ENST00000681639.1:n.1924T>C
ENST00000328194.7:c.3645T>C	ENSP00000328524.3:p.Asp1215=
ENST00000525784.5:c.581T>C
ENST00000527700.5:n.3207T>C
ENST00000528725.5:c.341T>C
ENST00000529977.5:n.1546T>C
ENST00000530044.5:c.3645T>C	ENSP00000435866.1:p.Asp1215=
ENST00000531747.1:c.881T>C
ENST00000533737.5:c.308T>C
NM_001243254.1:c.3645T>C	NP_001230183.1:p.Asp1215=
NM_015213.3:c.3645T>C	NP_056028.2:p.Asp1215=
XM_005252832.1:c.3645T>C	XP_005252889.1:p.Asp1215=
XM_011519952.1:c.3645T>C	XP_011518254.1:p.Asp1215=
XM_011519953.1:c.1743T>C	XP_011518255.1:p.Asp581=
XR_242782.2:n.3827T>C
XR_930851.1:n.3827T>C
NM_001348749.1:c.3573T>C	NP_001335678.1:p.Asp1191=
NM_001348750.1:c.3357T>C	NP_001335679.1:p.Asp1119=
NR_145966.2:n.3819T>C
NM_015213.4:c.3645T>C MANE Select	NP_056028.2:p.Asp1215=
NM_001243254.2:c.3645T>C	NP_001230183.1:p.Asp1215=
NM_001348749.2:c.3573T>C	NP_001335678.1:p.Asp1191=
NM_001348750.2:c.3357T>C	NP_001335679.1:p.Asp1119=