Canonical Allele Identifier: CA379598235

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163646T>C (hg19) ; chr11:g.9142099T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142099T>C , CM000673.2:g.9142099T>C	GRCh38
NC_000011.9:g.9163646T>C , CM000673.1:g.9163646T>C	GRCh37
NC_000011.8:g.9120222T>C	NCBI36
NG_053019.1:g.128237A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3521A>G MANE Select	ENSP00000328524.3:p.Gln1174Arg
ENST00000525784.6:n.1383A>G
ENST00000530780.2:c.*3347A>G	ENSP00000433925.1:n.*3347A>G
ENST00000531747.2:n.3192A>G
ENST00000679446.1:n.3442A>G
ENST00000679458.1:n.4922A>G
ENST00000679460.1:n.4583A>G
ENST00000679568.1:c.3521A>G	ENSP00000505860.1:p.Gln1174Arg
ENST00000679745.1:n.4026A>G
ENST00000679773.1:n.2682A>G
ENST00000679926.1:n.4823A>G
ENST00000679999.1:c.*578A>G	ENSP00000505198.1:n.*578A>G
ENST00000680252.1:c.3188A>G
ENST00000680294.1:c.3314A>G	ENSP00000506113.1:p.Gln1105Arg
ENST00000680358.1:n.2820A>G
ENST00000680470.1:c.*1302A>G	ENSP00000505975.1:n.*1302A>G
ENST00000680554.1:c.*54A>G	ENSP00000505621.1:n.*54A>G
ENST00000680576.1:n.4997A>G
ENST00000680599.1:n.3562A>G
ENST00000680742.1:c.*54A>G	ENSP00000505206.1:n.*54A>G
ENST00000680791.1:n.2405A>G
ENST00000680885.1:n.5223A>G
ENST00000681158.1:c.3105A>G
ENST00000681203.1:c.3449A>G	ENSP00000506456.1:p.Gln1150Arg
ENST00000681371.1:n.3393A>G
ENST00000681425.1:n.3999A>G
ENST00000681639.1:n.1800A>G
ENST00000328194.7:c.3521A>G	ENSP00000328524.3:p.Gln1174Arg
ENST00000525784.5:c.457A>G
ENST00000527700.5:n.3083A>G
ENST00000528725.5:c.217A>G
ENST00000529977.5:n.1422A>G
ENST00000530044.5:c.3521A>G	ENSP00000435866.1:p.Gln1174Arg
ENST00000531747.1:c.757A>G
ENST00000533737.5:c.184A>G
NM_001243254.1:c.3521A>G	NP_001230183.1:p.Gln1174Arg
NM_015213.3:c.3521A>G	NP_056028.2:p.Gln1174Arg
XM_005252832.1:c.3521A>G	XP_005252889.1:p.Gln1174Arg
XM_011519952.1:c.3521A>G	XP_011518254.1:p.Gln1174Arg
XM_011519953.1:c.1619A>G	XP_011518255.1:p.Gln540Arg
XR_242782.2:n.3703A>G
XR_930851.1:n.3703A>G
NM_001348749.1:c.3449A>G	NP_001335678.1:p.Gln1150Arg
NM_001348750.1:c.3233A>G	NP_001335679.1:p.Gln1078Arg
NR_145966.2:n.3695A>G
NM_015213.4:c.3521A>G MANE Select	NP_056028.2:p.Gln1174Arg
NM_001243254.2:c.3521A>G	NP_001230183.1:p.Gln1174Arg
NM_001348749.2:c.3449A>G	NP_001335678.1:p.Gln1150Arg
NM_001348750.2:c.3233A>G	NP_001335679.1:p.Gln1078Arg