Canonical Allele Identifier: CA379597610

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163553A>C (hg19) ; chr11:g.9142006A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142006A>C , CM000673.2:g.9142006A>C	GRCh38
NC_000011.9:g.9163553A>C , CM000673.1:g.9163553A>C	GRCh37
NC_000011.8:g.9120129A>C	NCBI36
NG_053019.1:g.128330T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3614T>G MANE Select	ENSP00000328524.3:p.Ile1205Ser
ENST00000525784.6:n.1476T>G
ENST00000530780.2:c.*3440T>G	ENSP00000433925.1:n.*3440T>G
ENST00000531747.2:n.3285T>G
ENST00000679446.1:n.3535T>G
ENST00000679458.1:n.5015T>G
ENST00000679460.1:n.4676T>G
ENST00000679568.1:c.3614T>G	ENSP00000505860.1:p.Ile1205Ser
ENST00000679745.1:n.4119T>G
ENST00000679773.1:n.2775T>G
ENST00000679926.1:n.4916T>G
ENST00000679999.1:c.*671T>G	ENSP00000505198.1:n.*671T>G
ENST00000680252.1:c.3281T>G
ENST00000680294.1:c.3407T>G	ENSP00000506113.1:p.Ile1136Ser
ENST00000680358.1:n.2913T>G
ENST00000680470.1:c.*1395T>G	ENSP00000505975.1:n.*1395T>G
ENST00000680554.1:c.*147T>G	ENSP00000505621.1:n.*147T>G
ENST00000680576.1:n.5090T>G
ENST00000680599.1:n.3655T>G
ENST00000680742.1:c.*147T>G	ENSP00000505206.1:n.*147T>G
ENST00000680791.1:n.2498T>G
ENST00000680885.1:n.5316T>G
ENST00000681158.1:c.3198T>G
ENST00000681203.1:c.3542T>G	ENSP00000506456.1:p.Ile1181Ser
ENST00000681371.1:n.3486T>G
ENST00000681425.1:n.4092T>G
ENST00000681639.1:n.1893T>G
ENST00000328194.7:c.3614T>G	ENSP00000328524.3:p.Ile1205Ser
ENST00000525784.5:c.550T>G
ENST00000527700.5:n.3176T>G
ENST00000528725.5:c.310T>G
ENST00000529977.5:n.1515T>G
ENST00000530044.5:c.3614T>G	ENSP00000435866.1:p.Ile1205Ser
ENST00000531747.1:c.850T>G
ENST00000533737.5:c.277T>G
NM_001243254.1:c.3614T>G	NP_001230183.1:p.Ile1205Ser
NM_015213.3:c.3614T>G	NP_056028.2:p.Ile1205Ser
XM_005252832.1:c.3614T>G	XP_005252889.1:p.Ile1205Ser
XM_011519952.1:c.3614T>G	XP_011518254.1:p.Ile1205Ser
XM_011519953.1:c.1712T>G	XP_011518255.1:p.Ile571Ser
XR_242782.2:n.3796T>G
XR_930851.1:n.3796T>G
NM_001348749.1:c.3542T>G	NP_001335678.1:p.Ile1181Ser
NM_001348750.1:c.3326T>G	NP_001335679.1:p.Ile1109Ser
NR_145966.2:n.3788T>G
NM_015213.4:c.3614T>G MANE Select	NP_056028.2:p.Ile1205Ser
NM_001243254.2:c.3614T>G	NP_001230183.1:p.Ile1205Ser
NM_001348749.2:c.3542T>G	NP_001335678.1:p.Ile1181Ser
NM_001348750.2:c.3326T>G	NP_001335679.1:p.Ile1109Ser