Canonical Allele Identifier: CA379608485

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9182377T>G (hg19) ; chr11:g.9160830T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160830T>G , CM000673.2:g.9160830T>G	GRCh38
NC_000011.9:g.9182377T>G , CM000673.1:g.9182377T>G	GRCh37
NC_000011.8:g.9138953T>G	NCBI36
NG_053019.1:g.109506A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2319A>C MANE Select	ENSP00000328524.3:p.Glu773Asp
ENST00000530780.2:c.*2145A>C	ENSP00000433925.1:n.*2145A>C
ENST00000679446.1:n.2240A>C
ENST00000679458.1:n.3720A>C
ENST00000679460.1:n.2108A>C
ENST00000679568.1:c.2319A>C	ENSP00000505860.1:p.Glu773Asp
ENST00000679745.1:n.2108A>C
ENST00000679926.1:n.1135A>C
ENST00000679999.1:c.2319A>C	ENSP00000505198.1:p.Glu773Asp
ENST00000680252.1:c.2108A>C
ENST00000680294.1:c.2319A>C	ENSP00000506113.1:p.Glu773Asp
ENST00000680358.1:n.1618A>C
ENST00000680470.1:c.*185A>C	ENSP00000505975.1:n.*185A>C
ENST00000680554.1:c.2031A>C	ENSP00000505621.1:p.Glu677Asp
ENST00000680576.1:n.2108A>C
ENST00000680599.1:n.2236A>C
ENST00000680742.1:c.2319A>C	ENSP00000505206.1:p.Glu773Asp
ENST00000680885.1:n.2240A>C
ENST00000681158.1:c.2108A>C
ENST00000681173.1:n.2108A>C
ENST00000681203.1:c.2247A>C	ENSP00000506456.1:p.Glu749Asp
ENST00000681425.1:n.2240A>C
ENST00000328194.7:c.2319A>C	ENSP00000328524.3:p.Glu773Asp
ENST00000526707.5:c.2247A>C	ENSP00000436780.1:p.Glu749Asp
ENST00000527700.5:n.1881A>C
ENST00000530044.5:c.2319A>C	ENSP00000435866.1:p.Glu773Asp
NM_001243254.1:c.2319A>C	NP_001230183.1:p.Glu773Asp
NM_015213.3:c.2319A>C	NP_056028.2:p.Glu773Asp
XM_005252832.1:c.2319A>C	XP_005252889.1:p.Glu773Asp
XM_011519952.1:c.2319A>C	XP_011518254.1:p.Glu773Asp
XM_011519953.1:c.417A>C	XP_011518255.1:p.Glu139Asp
XR_242782.2:n.2584A>C
XR_930851.1:n.2584A>C
XR_930852.1:n.2584A>C
XR_930853.1:n.2433A>C
NM_001348749.1:c.2247A>C	NP_001335678.1:p.Glu749Asp
NM_001348750.1:c.2031A>C	NP_001335679.1:p.Glu677Asp
NR_145966.2:n.2576A>C
NM_015213.4:c.2319A>C MANE Select	NP_056028.2:p.Glu773Asp
NM_001243254.2:c.2319A>C	NP_001230183.1:p.Glu773Asp
NM_001348749.2:c.2247A>C	NP_001335678.1:p.Glu749Asp
NM_001348750.2:c.2031A>C	NP_001335679.1:p.Glu677Asp