Canonical Allele Identifier: CA379597123

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163494C>G (hg19) ; chr11:g.9141947C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141947C>G , CM000673.2:g.9141947C>G	GRCh38
NC_000011.9:g.9163494C>G , CM000673.1:g.9163494C>G	GRCh37
NC_000011.8:g.9120070C>G	NCBI36
NG_053019.1:g.128389G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3673G>C MANE Select	ENSP00000328524.3:p.Gly1225Arg
ENST00000525784.6:n.1535G>C
ENST00000530780.2:c.*3499G>C	ENSP00000433925.1:n.*3499G>C
ENST00000531747.2:n.3344G>C
ENST00000679446.1:n.3594G>C
ENST00000679458.1:n.5074G>C
ENST00000679460.1:n.4735G>C
ENST00000679568.1:c.3673G>C	ENSP00000505860.1:p.Gly1225Arg
ENST00000679745.1:n.4178G>C
ENST00000679773.1:n.2834G>C
ENST00000679926.1:n.4975G>C
ENST00000679999.1:c.*730G>C	ENSP00000505198.1:n.*730G>C
ENST00000680252.1:c.3340G>C
ENST00000680294.1:c.3466G>C	ENSP00000506113.1:p.Gly1156Arg
ENST00000680358.1:n.2972G>C
ENST00000680470.1:c.*1454G>C	ENSP00000505975.1:n.*1454G>C
ENST00000680554.1:c.*206G>C	ENSP00000505621.1:n.*206G>C
ENST00000680576.1:n.5149G>C
ENST00000680599.1:n.3714G>C
ENST00000680742.1:c.*179+27G>C	ENSP00000505206.1:n.*179+27G>C
ENST00000680791.1:n.2557G>C
ENST00000680885.1:n.5375G>C
ENST00000681158.1:c.3257G>C
ENST00000681203.1:c.3601G>C	ENSP00000506456.1:p.Gly1201Arg
ENST00000681371.1:n.3545G>C
ENST00000681425.1:n.4151G>C
ENST00000681639.1:n.1952G>C
ENST00000328194.7:c.3673G>C	ENSP00000328524.3:p.Gly1225Arg
ENST00000525784.5:c.609G>C
ENST00000527700.5:n.3235G>C
ENST00000528725.5:c.369G>C
ENST00000529977.5:n.1574G>C
ENST00000530044.5:c.3646+27G>C	ENSP00000435866.1:n.3646+27G>C
ENST00000531747.1:c.909G>C
ENST00000533737.5:c.336G>C
NM_001243254.1:c.3646+27G>C	NP_001230183.1:n.3646+27G>C
NM_015213.3:c.3673G>C	NP_056028.2:p.Gly1225Arg
XM_005252832.1:c.3673G>C	XP_005252889.1:p.Gly1225Arg
XM_011519952.1:c.3646+27G>C	XP_011518254.1:n.3646+27G>C
XM_011519953.1:c.1771G>C	XP_011518255.1:p.Gly591Arg
XR_242782.2:n.3855G>C
XR_930851.1:n.3828+27G>C
NM_001348749.1:c.3601G>C	NP_001335678.1:p.Gly1201Arg
NM_001348750.1:c.3385G>C	NP_001335679.1:p.Gly1129Arg
NR_145966.2:n.3847G>C
NM_015213.4:c.3673G>C MANE Select	NP_056028.2:p.Gly1225Arg
NM_001243254.2:c.3646+27G>C	NP_001230183.1:n.3646+27G>C
NM_001348749.2:c.3601G>C	NP_001335678.1:p.Gly1201Arg
NM_001348750.2:c.3385G>C	NP_001335679.1:p.Gly1129Arg