Canonical Allele Identifier: CA379597507

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163538C>G (hg19) ; chr11:g.9141991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141991C>G , CM000673.2:g.9141991C>G	GRCh38
NC_000011.9:g.9163538C>G , CM000673.1:g.9163538C>G	GRCh37
NC_000011.8:g.9120114C>G	NCBI36
NG_053019.1:g.128345G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3629G>C MANE Select	ENSP00000328524.3:p.Arg1210Pro
ENST00000525784.6:n.1491G>C
ENST00000530780.2:c.*3455G>C	ENSP00000433925.1:n.*3455G>C
ENST00000531747.2:n.3300G>C
ENST00000679446.1:n.3550G>C
ENST00000679458.1:n.5030G>C
ENST00000679460.1:n.4691G>C
ENST00000679568.1:c.3629G>C	ENSP00000505860.1:p.Arg1210Pro
ENST00000679745.1:n.4134G>C
ENST00000679773.1:n.2790G>C
ENST00000679926.1:n.4931G>C
ENST00000679999.1:c.*686G>C	ENSP00000505198.1:n.*686G>C
ENST00000680252.1:c.3296G>C
ENST00000680294.1:c.3422G>C	ENSP00000506113.1:p.Arg1141Pro
ENST00000680358.1:n.2928G>C
ENST00000680470.1:c.*1410G>C	ENSP00000505975.1:n.*1410G>C
ENST00000680554.1:c.*162G>C	ENSP00000505621.1:n.*162G>C
ENST00000680576.1:n.5105G>C
ENST00000680599.1:n.3670G>C
ENST00000680742.1:c.*162G>C	ENSP00000505206.1:n.*162G>C
ENST00000680791.1:n.2513G>C
ENST00000680885.1:n.5331G>C
ENST00000681158.1:c.3213G>C
ENST00000681203.1:c.3557G>C	ENSP00000506456.1:p.Arg1186Pro
ENST00000681371.1:n.3501G>C
ENST00000681425.1:n.4107G>C
ENST00000681639.1:n.1908G>C
ENST00000328194.7:c.3629G>C	ENSP00000328524.3:p.Arg1210Pro
ENST00000525784.5:c.565G>C
ENST00000527700.5:n.3191G>C
ENST00000528725.5:c.325G>C
ENST00000529977.5:n.1530G>C
ENST00000530044.5:c.3629G>C	ENSP00000435866.1:p.Arg1210Pro
ENST00000531747.1:c.865G>C
ENST00000533737.5:c.292G>C
NM_001243254.1:c.3629G>C	NP_001230183.1:p.Arg1210Pro
NM_015213.3:c.3629G>C	NP_056028.2:p.Arg1210Pro
XM_005252832.1:c.3629G>C	XP_005252889.1:p.Arg1210Pro
XM_011519952.1:c.3629G>C	XP_011518254.1:p.Arg1210Pro
XM_011519953.1:c.1727G>C	XP_011518255.1:p.Arg576Pro
XR_242782.2:n.3811G>C
XR_930851.1:n.3811G>C
NM_001348749.1:c.3557G>C	NP_001335678.1:p.Arg1186Pro
NM_001348750.1:c.3341G>C	NP_001335679.1:p.Arg1114Pro
NR_145966.2:n.3803G>C
NM_015213.4:c.3629G>C MANE Select	NP_056028.2:p.Arg1210Pro
NM_001243254.2:c.3629G>C	NP_001230183.1:p.Arg1210Pro
NM_001348749.2:c.3557G>C	NP_001335678.1:p.Arg1186Pro
NM_001348750.2:c.3341G>C	NP_001335679.1:p.Arg1114Pro