Canonical Allele Identifier: CA379597120

Gene: DENND5A

Linked Data

• dbSNP Id: rs1554909065
• MyVariant Identifiers: chr11:g.9163494C>A (hg19) ; chr11:g.9141947C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3673G>T MANE Select	ENSP00000328524.3:p.Gly1225Ter
ENST00000525784.6:n.1535G>T
ENST00000530780.2:c.*3499G>T	ENSP00000433925.1:n.*3499G>T
ENST00000531747.2:n.3344G>T
ENST00000679446.1:n.3594G>T
ENST00000679458.1:n.5074G>T
ENST00000679460.1:n.4735G>T
ENST00000679568.1:c.3673G>T	ENSP00000505860.1:p.Gly1225Ter
ENST00000679745.1:n.4178G>T
ENST00000679773.1:n.2834G>T
ENST00000679926.1:n.4975G>T
ENST00000679999.1:c.*730G>T	ENSP00000505198.1:n.*730G>T
ENST00000680252.1:c.3340G>T
ENST00000680294.1:c.3466G>T	ENSP00000506113.1:p.Gly1156Ter
ENST00000680358.1:n.2972G>T
ENST00000680470.1:c.*1454G>T	ENSP00000505975.1:n.*1454G>T
ENST00000680554.1:c.*206G>T	ENSP00000505621.1:n.*206G>T
ENST00000680576.1:n.5149G>T
ENST00000680599.1:n.3714G>T
ENST00000680742.1:c.*179+27G>T	ENSP00000505206.1:n.*179+27G>T
ENST00000680791.1:n.2557G>T
ENST00000680885.1:n.5375G>T
ENST00000681158.1:c.3257G>T
ENST00000681203.1:c.3601G>T	ENSP00000506456.1:p.Gly1201Ter
ENST00000681371.1:n.3545G>T
ENST00000681425.1:n.4151G>T
ENST00000681639.1:n.1952G>T
ENST00000328194.7:c.3673G>T	ENSP00000328524.3:p.Gly1225Ter
ENST00000525784.5:c.609G>T
ENST00000527700.5:n.3235G>T
ENST00000528725.5:c.369G>T
ENST00000529977.5:n.1574G>T
ENST00000530044.5:c.3646+27G>T	ENSP00000435866.1:n.3646+27G>T
ENST00000531747.1:c.909G>T
ENST00000533737.5:c.336G>T
NM_001243254.1:c.3646+27G>T	NP_001230183.1:n.3646+27G>T
NM_015213.3:c.3673G>T	NP_056028.2:p.Gly1225Ter
XM_005252832.1:c.3673G>T	XP_005252889.1:p.Gly1225Ter
XM_011519952.1:c.3646+27G>T	XP_011518254.1:n.3646+27G>T
XM_011519953.1:c.1771G>T	XP_011518255.1:p.Gly591Ter
XR_242782.2:n.3855G>T
XR_930851.1:n.3828+27G>T
NM_001348749.1:c.3601G>T	NP_001335678.1:p.Gly1201Ter
NM_001348750.1:c.3385G>T	NP_001335679.1:p.Gly1129Ter
NR_145966.2:n.3847G>T
NM_015213.4:c.3673G>T MANE Select	NP_056028.2:p.Gly1225Ter
NM_001243254.2:c.3646+27G>T	NP_001230183.1:n.3646+27G>T
NM_001348749.2:c.3601G>T	NP_001335678.1:p.Gly1201Ter
NM_001348750.2:c.3385G>T	NP_001335679.1:p.Gly1129Ter