Canonical Allele Identifier: CA379597575

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163548T>C (hg19) ; chr11:g.9142001T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142001T>C , CM000673.2:g.9142001T>C	GRCh38
NC_000011.9:g.9163548T>C , CM000673.1:g.9163548T>C	GRCh37
NC_000011.8:g.9120124T>C	NCBI36
NG_053019.1:g.128335A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3619A>G MANE Select	ENSP00000328524.3:p.Asn1207Asp
ENST00000525784.6:n.1481A>G
ENST00000530780.2:c.*3445A>G	ENSP00000433925.1:n.*3445A>G
ENST00000531747.2:n.3290A>G
ENST00000679446.1:n.3540A>G
ENST00000679458.1:n.5020A>G
ENST00000679460.1:n.4681A>G
ENST00000679568.1:c.3619A>G	ENSP00000505860.1:p.Asn1207Asp
ENST00000679745.1:n.4124A>G
ENST00000679773.1:n.2780A>G
ENST00000679926.1:n.4921A>G
ENST00000679999.1:c.*676A>G	ENSP00000505198.1:n.*676A>G
ENST00000680252.1:c.3286A>G
ENST00000680294.1:c.3412A>G	ENSP00000506113.1:p.Asn1138Asp
ENST00000680358.1:n.2918A>G
ENST00000680470.1:c.*1400A>G	ENSP00000505975.1:n.*1400A>G
ENST00000680554.1:c.*152A>G	ENSP00000505621.1:n.*152A>G
ENST00000680576.1:n.5095A>G
ENST00000680599.1:n.3660A>G
ENST00000680742.1:c.*152A>G	ENSP00000505206.1:n.*152A>G
ENST00000680791.1:n.2503A>G
ENST00000680885.1:n.5321A>G
ENST00000681158.1:c.3203A>G
ENST00000681203.1:c.3547A>G	ENSP00000506456.1:p.Asn1183Asp
ENST00000681371.1:n.3491A>G
ENST00000681425.1:n.4097A>G
ENST00000681639.1:n.1898A>G
ENST00000328194.7:c.3619A>G	ENSP00000328524.3:p.Asn1207Asp
ENST00000525784.5:c.555A>G
ENST00000527700.5:n.3181A>G
ENST00000528725.5:c.315A>G
ENST00000529977.5:n.1520A>G
ENST00000530044.5:c.3619A>G	ENSP00000435866.1:p.Asn1207Asp
ENST00000531747.1:c.855A>G
ENST00000533737.5:c.282A>G
NM_001243254.1:c.3619A>G	NP_001230183.1:p.Asn1207Asp
NM_015213.3:c.3619A>G	NP_056028.2:p.Asn1207Asp
XM_005252832.1:c.3619A>G	XP_005252889.1:p.Asn1207Asp
XM_011519952.1:c.3619A>G	XP_011518254.1:p.Asn1207Asp
XM_011519953.1:c.1717A>G	XP_011518255.1:p.Asn573Asp
XR_242782.2:n.3801A>G
XR_930851.1:n.3801A>G
NM_001348749.1:c.3547A>G	NP_001335678.1:p.Asn1183Asp
NM_001348750.1:c.3331A>G	NP_001335679.1:p.Asn1111Asp
NR_145966.2:n.3793A>G
NM_015213.4:c.3619A>G MANE Select	NP_056028.2:p.Asn1207Asp
NM_001243254.2:c.3619A>G	NP_001230183.1:p.Asn1207Asp
NM_001348749.2:c.3547A>G	NP_001335678.1:p.Asn1183Asp
NM_001348750.2:c.3331A>G	NP_001335679.1:p.Asn1111Asp