Canonical Allele Identifier: CA379597331

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163524C>G (hg19) ; chr11:g.9141977C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141977C>G , CM000673.2:g.9141977C>G	GRCh38
NC_000011.9:g.9163524C>G , CM000673.1:g.9163524C>G	GRCh37
NC_000011.8:g.9120100C>G	NCBI36
NG_053019.1:g.128359G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3643G>C MANE Select	ENSP00000328524.3:p.Asp1215His
ENST00000525784.6:n.1505G>C
ENST00000530780.2:c.*3469G>C	ENSP00000433925.1:n.*3469G>C
ENST00000531747.2:n.3314G>C
ENST00000679446.1:n.3564G>C
ENST00000679458.1:n.5044G>C
ENST00000679460.1:n.4705G>C
ENST00000679568.1:c.3643G>C	ENSP00000505860.1:p.Asp1215His
ENST00000679745.1:n.4148G>C
ENST00000679773.1:n.2804G>C
ENST00000679926.1:n.4945G>C
ENST00000679999.1:c.*700G>C	ENSP00000505198.1:n.*700G>C
ENST00000680252.1:c.3310G>C
ENST00000680294.1:c.3436G>C	ENSP00000506113.1:p.Asp1146His
ENST00000680358.1:n.2942G>C
ENST00000680470.1:c.*1424G>C	ENSP00000505975.1:n.*1424G>C
ENST00000680554.1:c.*176G>C	ENSP00000505621.1:n.*176G>C
ENST00000680576.1:n.5119G>C
ENST00000680599.1:n.3684G>C
ENST00000680742.1:c.*176G>C	ENSP00000505206.1:n.*176G>C
ENST00000680791.1:n.2527G>C
ENST00000680885.1:n.5345G>C
ENST00000681158.1:c.3227G>C
ENST00000681203.1:c.3571G>C	ENSP00000506456.1:p.Asp1191His
ENST00000681371.1:n.3515G>C
ENST00000681425.1:n.4121G>C
ENST00000681639.1:n.1922G>C
ENST00000328194.7:c.3643G>C	ENSP00000328524.3:p.Asp1215His
ENST00000525784.5:c.579G>C
ENST00000527700.5:n.3205G>C
ENST00000528725.5:c.339G>C
ENST00000529977.5:n.1544G>C
ENST00000530044.5:c.3643G>C	ENSP00000435866.1:p.Asp1215His
ENST00000531747.1:c.879G>C
ENST00000533737.5:c.306G>C
NM_001243254.1:c.3643G>C	NP_001230183.1:p.Asp1215His
NM_015213.3:c.3643G>C	NP_056028.2:p.Asp1215His
XM_005252832.1:c.3643G>C	XP_005252889.1:p.Asp1215His
XM_011519952.1:c.3643G>C	XP_011518254.1:p.Asp1215His
XM_011519953.1:c.1741G>C	XP_011518255.1:p.Asp581His
XR_242782.2:n.3825G>C
XR_930851.1:n.3825G>C
NM_001348749.1:c.3571G>C	NP_001335678.1:p.Asp1191His
NM_001348750.1:c.3355G>C	NP_001335679.1:p.Asp1119His
NR_145966.2:n.3817G>C
NM_015213.4:c.3643G>C MANE Select	NP_056028.2:p.Asp1215His
NM_001243254.2:c.3643G>C	NP_001230183.1:p.Asp1215His
NM_001348749.2:c.3571G>C	NP_001335678.1:p.Asp1191His
NM_001348750.2:c.3355G>C	NP_001335679.1:p.Asp1119His