Canonical Allele Identifier: CA379599704

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9225663G>C (hg19) ; chr11:g.9204116G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204116G>C , CM000673.2:g.9204116G>C	GRCh38
NC_000011.9:g.9225663G>C , CM000673.1:g.9225663G>C	GRCh37
NC_000011.8:g.9182239G>C	NCBI36
NG_053019.1:g.66220C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.493C>G MANE Select	ENSP00000328524.3:p.His165Asp
ENST00000530780.2:c.*319C>G	ENSP00000433925.1:n.*319C>G
ENST00000530867.2:n.282C>G
ENST00000532696.2:n.416C>G
ENST00000679446.1:n.414C>G
ENST00000679460.1:n.282C>G
ENST00000679568.1:c.493C>G	ENSP00000505860.1:p.His165Asp
ENST00000679745.1:n.282C>G
ENST00000679999.1:c.493C>G	ENSP00000505198.1:p.His165Asp
ENST00000680252.1:c.282C>G
ENST00000680294.1:c.493C>G	ENSP00000506113.1:p.His165Asp
ENST00000680470.1:c.493C>G	ENSP00000505975.1:p.His165Asp
ENST00000680554.1:c.205C>G	ENSP00000505621.1:p.His69Asp
ENST00000680576.1:n.282C>G
ENST00000680599.1:n.410C>G
ENST00000680742.1:c.493C>G	ENSP00000505206.1:p.His165Asp
ENST00000680885.1:n.414C>G
ENST00000681158.1:c.282C>G
ENST00000681173.1:n.282C>G
ENST00000681203.1:c.421C>G	ENSP00000506456.1:p.His141Asp
ENST00000681425.1:n.414C>G
ENST00000681915.1:n.282C>G
ENST00000328194.7:c.493C>G	ENSP00000328524.3:p.His165Asp
ENST00000526707.5:c.421C>G	ENSP00000436780.1:p.His141Asp
ENST00000530044.5:c.493C>G	ENSP00000435866.1:p.His165Asp
ENST00000530780.1:c.*319C>G	ENSP00000433925.1:n.*319C>G
ENST00000532696.1:n.248C>G
NM_001243254.1:c.493C>G	NP_001230183.1:p.His165Asp
NM_015213.3:c.493C>G	NP_056028.2:p.His165Asp
XM_005252832.1:c.493C>G	XP_005252889.1:p.His165Asp
XM_011519952.1:c.493C>G	XP_011518254.1:p.His165Asp
XR_242782.2:n.758C>G
XR_930851.1:n.758C>G
XR_930852.1:n.758C>G
XR_930853.1:n.758C>G
NM_001348749.1:c.421C>G	NP_001335678.1:p.His141Asp
NM_001348750.1:c.205C>G	NP_001335679.1:p.His69Asp
NR_145966.2:n.750C>G
NM_015213.4:c.493C>G MANE Select	NP_056028.2:p.His165Asp
NM_001243254.2:c.493C>G	NP_001230183.1:p.His165Asp
NM_001348749.2:c.421C>G	NP_001335678.1:p.His141Asp
NM_001348750.2:c.205C>G	NP_001335679.1:p.His69Asp