Canonical Allele Identifier: CA379597512

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163539G>C (hg19) ; chr11:g.9141992G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141992G>C , CM000673.2:g.9141992G>C	GRCh38
NC_000011.9:g.9163539G>C , CM000673.1:g.9163539G>C	GRCh37
NC_000011.8:g.9120115G>C	NCBI36
NG_053019.1:g.128344C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3628C>G MANE Select	ENSP00000328524.3:p.Arg1210Gly
ENST00000525784.6:n.1490C>G
ENST00000530780.2:c.*3454C>G	ENSP00000433925.1:n.*3454C>G
ENST00000531747.2:n.3299C>G
ENST00000679446.1:n.3549C>G
ENST00000679458.1:n.5029C>G
ENST00000679460.1:n.4690C>G
ENST00000679568.1:c.3628C>G	ENSP00000505860.1:p.Arg1210Gly
ENST00000679745.1:n.4133C>G
ENST00000679773.1:n.2789C>G
ENST00000679926.1:n.4930C>G
ENST00000679999.1:c.*685C>G	ENSP00000505198.1:n.*685C>G
ENST00000680252.1:c.3295C>G
ENST00000680294.1:c.3421C>G	ENSP00000506113.1:p.Arg1141Gly
ENST00000680358.1:n.2927C>G
ENST00000680470.1:c.*1409C>G	ENSP00000505975.1:n.*1409C>G
ENST00000680554.1:c.*161C>G	ENSP00000505621.1:n.*161C>G
ENST00000680576.1:n.5104C>G
ENST00000680599.1:n.3669C>G
ENST00000680742.1:c.*161C>G	ENSP00000505206.1:n.*161C>G
ENST00000680791.1:n.2512C>G
ENST00000680885.1:n.5330C>G
ENST00000681158.1:c.3212C>G
ENST00000681203.1:c.3556C>G	ENSP00000506456.1:p.Arg1186Gly
ENST00000681371.1:n.3500C>G
ENST00000681425.1:n.4106C>G
ENST00000681639.1:n.1907C>G
ENST00000328194.7:c.3628C>G	ENSP00000328524.3:p.Arg1210Gly
ENST00000525784.5:c.564C>G
ENST00000527700.5:n.3190C>G
ENST00000528725.5:c.324C>G
ENST00000529977.5:n.1529C>G
ENST00000530044.5:c.3628C>G	ENSP00000435866.1:p.Arg1210Gly
ENST00000531747.1:c.864C>G
ENST00000533737.5:c.291C>G
NM_001243254.1:c.3628C>G	NP_001230183.1:p.Arg1210Gly
NM_015213.3:c.3628C>G	NP_056028.2:p.Arg1210Gly
XM_005252832.1:c.3628C>G	XP_005252889.1:p.Arg1210Gly
XM_011519952.1:c.3628C>G	XP_011518254.1:p.Arg1210Gly
XM_011519953.1:c.1726C>G	XP_011518255.1:p.Arg576Gly
XR_242782.2:n.3810C>G
XR_930851.1:n.3810C>G
NM_001348749.1:c.3556C>G	NP_001335678.1:p.Arg1186Gly
NM_001348750.1:c.3340C>G	NP_001335679.1:p.Arg1114Gly
NR_145966.2:n.3802C>G
NM_015213.4:c.3628C>G MANE Select	NP_056028.2:p.Arg1210Gly
NM_001243254.2:c.3628C>G	NP_001230183.1:p.Arg1210Gly
NM_001348749.2:c.3556C>G	NP_001335678.1:p.Arg1186Gly
NM_001348750.2:c.3340C>G	NP_001335679.1:p.Arg1114Gly