Canonical Allele Identifier: CA379608160

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9182332T>G (hg19) ; chr11:g.9160785T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160785T>G , CM000673.2:g.9160785T>G	GRCh38
NC_000011.9:g.9182332T>G , CM000673.1:g.9182332T>G	GRCh37
NC_000011.8:g.9138908T>G	NCBI36
NG_053019.1:g.109551A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2364A>C MANE Select	ENSP00000328524.3:p.Glu788Asp
ENST00000530780.2:c.*2190A>C	ENSP00000433925.1:n.*2190A>C
ENST00000679446.1:n.2285A>C
ENST00000679458.1:n.3765A>C
ENST00000679460.1:n.2153A>C
ENST00000679568.1:c.2364A>C	ENSP00000505860.1:p.Glu788Asp
ENST00000679745.1:n.2153A>C
ENST00000679926.1:n.1180A>C
ENST00000679999.1:c.2364A>C	ENSP00000505198.1:p.Glu788Asp
ENST00000680252.1:c.2153A>C
ENST00000680294.1:c.2364A>C	ENSP00000506113.1:p.Glu788Asp
ENST00000680358.1:n.1663A>C
ENST00000680470.1:c.*230A>C	ENSP00000505975.1:n.*230A>C
ENST00000680554.1:c.2076A>C	ENSP00000505621.1:p.Glu692Asp
ENST00000680576.1:n.2153A>C
ENST00000680599.1:n.2281A>C
ENST00000680742.1:c.2364A>C	ENSP00000505206.1:p.Glu788Asp
ENST00000680885.1:n.2285A>C
ENST00000681158.1:c.2153A>C
ENST00000681173.1:n.2153A>C
ENST00000681203.1:c.2292A>C	ENSP00000506456.1:p.Glu764Asp
ENST00000681425.1:n.2285A>C
ENST00000328194.7:c.2364A>C	ENSP00000328524.3:p.Glu788Asp
ENST00000526707.5:c.2292A>C	ENSP00000436780.1:p.Glu764Asp
ENST00000527700.5:n.1926A>C
ENST00000530044.5:c.2364A>C	ENSP00000435866.1:p.Glu788Asp
NM_001243254.1:c.2364A>C	NP_001230183.1:p.Glu788Asp
NM_015213.3:c.2364A>C	NP_056028.2:p.Glu788Asp
XM_005252832.1:c.2364A>C	XP_005252889.1:p.Glu788Asp
XM_011519952.1:c.2364A>C	XP_011518254.1:p.Glu788Asp
XM_011519953.1:c.462A>C	XP_011518255.1:p.Glu154Asp
XR_242782.2:n.2629A>C
XR_930851.1:n.2629A>C
XR_930852.1:n.2629A>C
XR_930853.1:n.2478A>C
NM_001348749.1:c.2292A>C	NP_001335678.1:p.Glu764Asp
NM_001348750.1:c.2076A>C	NP_001335679.1:p.Glu692Asp
NR_145966.2:n.2621A>C
NM_015213.4:c.2364A>C MANE Select	NP_056028.2:p.Glu788Asp
NM_001243254.2:c.2364A>C	NP_001230183.1:p.Glu788Asp
NM_001348749.2:c.2292A>C	NP_001335678.1:p.Glu764Asp
NM_001348750.2:c.2076A>C	NP_001335679.1:p.Glu692Asp