Canonical Allele Identifier: CA379597474

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163535T>G (hg19) ; chr11:g.9141988T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141988T>G , CM000673.2:g.9141988T>G	GRCh38
NC_000011.9:g.9163535T>G , CM000673.1:g.9163535T>G	GRCh37
NC_000011.8:g.9120111T>G	NCBI36
NG_053019.1:g.128348A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3632A>C MANE Select	ENSP00000328524.3:p.Asn1211Thr
ENST00000525784.6:n.1494A>C
ENST00000530780.2:c.*3458A>C	ENSP00000433925.1:n.*3458A>C
ENST00000531747.2:n.3303A>C
ENST00000679446.1:n.3553A>C
ENST00000679458.1:n.5033A>C
ENST00000679460.1:n.4694A>C
ENST00000679568.1:c.3632A>C	ENSP00000505860.1:p.Asn1211Thr
ENST00000679745.1:n.4137A>C
ENST00000679773.1:n.2793A>C
ENST00000679926.1:n.4934A>C
ENST00000679999.1:c.*689A>C	ENSP00000505198.1:n.*689A>C
ENST00000680252.1:c.3299A>C
ENST00000680294.1:c.3425A>C	ENSP00000506113.1:p.Asn1142Thr
ENST00000680358.1:n.2931A>C
ENST00000680470.1:c.*1413A>C	ENSP00000505975.1:n.*1413A>C
ENST00000680554.1:c.*165A>C	ENSP00000505621.1:n.*165A>C
ENST00000680576.1:n.5108A>C
ENST00000680599.1:n.3673A>C
ENST00000680742.1:c.*165A>C	ENSP00000505206.1:n.*165A>C
ENST00000680791.1:n.2516A>C
ENST00000680885.1:n.5334A>C
ENST00000681158.1:c.3216A>C
ENST00000681203.1:c.3560A>C	ENSP00000506456.1:p.Asn1187Thr
ENST00000681371.1:n.3504A>C
ENST00000681425.1:n.4110A>C
ENST00000681639.1:n.1911A>C
ENST00000328194.7:c.3632A>C	ENSP00000328524.3:p.Asn1211Thr
ENST00000525784.5:c.568A>C
ENST00000527700.5:n.3194A>C
ENST00000528725.5:c.328A>C
ENST00000529977.5:n.1533A>C
ENST00000530044.5:c.3632A>C	ENSP00000435866.1:p.Asn1211Thr
ENST00000531747.1:c.868A>C
ENST00000533737.5:c.295A>C
NM_001243254.1:c.3632A>C	NP_001230183.1:p.Asn1211Thr
NM_015213.3:c.3632A>C	NP_056028.2:p.Asn1211Thr
XM_005252832.1:c.3632A>C	XP_005252889.1:p.Asn1211Thr
XM_011519952.1:c.3632A>C	XP_011518254.1:p.Asn1211Thr
XM_011519953.1:c.1730A>C	XP_011518255.1:p.Asn577Thr
XR_242782.2:n.3814A>C
XR_930851.1:n.3814A>C
NM_001348749.1:c.3560A>C	NP_001335678.1:p.Asn1187Thr
NM_001348750.1:c.3344A>C	NP_001335679.1:p.Asn1115Thr
NR_145966.2:n.3806A>C
NM_015213.4:c.3632A>C MANE Select	NP_056028.2:p.Asn1211Thr
NM_001243254.2:c.3632A>C	NP_001230183.1:p.Asn1211Thr
NM_001348749.2:c.3560A>C	NP_001335678.1:p.Asn1187Thr
NM_001348750.2:c.3344A>C	NP_001335679.1:p.Asn1115Thr