Canonical Allele Identifier: CA2790381953

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141949_9141951del , CM000673.2:g.9141949_9141951del	GRCh38
NC_000011.9:g.9163496_9163498del , CM000673.1:g.9163496_9163498del	GRCh37
NC_000011.8:g.9120072_9120074del	NCBI36
NG_053019.1:g.128385_128387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3669_3671del MANE Select	ENSP00000328524.3:p.Cys1223_Leu1224delinsTrp
ENST00000525784.6:n.1531_1533del
ENST00000530780.2:c.*3495_*3497del	ENSP00000433925.1:n.*3495_*3497del
ENST00000531747.2:n.3340_3342del
ENST00000679446.1:n.3590_3592del
ENST00000679458.1:n.5070_5072del
ENST00000679460.1:n.4731_4733del
ENST00000679568.1:c.3669_3671del	ENSP00000505860.1:p.Cys1223_Leu1224delinsTrp
ENST00000679745.1:n.4174_4176del
ENST00000679773.1:n.2830_2832del
ENST00000679926.1:n.4971_4973del
ENST00000679999.1:c.*726_*728del	ENSP00000505198.1:n.*726_*728del
ENST00000680252.1:c.3336_3338del
ENST00000680294.1:c.3462_3464del	ENSP00000506113.1:p.Cys1154_Leu1155delinsTrp
ENST00000680358.1:n.2968_2970del
ENST00000680470.1:c.*1450_*1452del	ENSP00000505975.1:n.*1450_*1452del
ENST00000680554.1:c.*202_*204del	ENSP00000505621.1:n.*202_*204del
ENST00000680576.1:n.5145_5147del
ENST00000680599.1:n.3710_3712del
ENST00000680742.1:c.*179+23_*179+25del	ENSP00000505206.1:n.*179+23_*179+25del
ENST00000680791.1:n.2553_2555del
ENST00000680885.1:n.5371_5373del
ENST00000681158.1:c.3253_3255del
ENST00000681203.1:c.3597_3599del	ENSP00000506456.1:p.Cys1199_Leu1200delinsTrp
ENST00000681371.1:n.3541_3543del
ENST00000681425.1:n.4147_4149del
ENST00000681639.1:n.1948_1950del
ENST00000328194.7:c.3669_3671del	ENSP00000328524.3:p.Cys1223_Leu1224delinsTrp
ENST00000525784.5:c.605_607del
ENST00000527700.5:n.3231_3233del
ENST00000528725.5:c.365_367del
ENST00000529977.5:n.1570_1572del
ENST00000530044.5:c.3646+23_3646+25del	ENSP00000435866.1:n.3646+23_3646+25del
ENST00000531747.1:c.905_907del
ENST00000533737.5:c.332_334del
NM_001243254.1:c.3646+23_3646+25del	NP_001230183.1:n.3646+23_3646+25del
NM_015213.3:c.3669_3671del	NP_056028.2:p.Cys1223_Leu1224delinsTrp
XM_005252832.1:c.3669_3671del	XP_005252889.1:p.Cys1223_Leu1224delinsTrp
XM_011519952.1:c.3646+23_3646+25del	XP_011518254.1:n.3646+23_3646+25del
XM_011519953.1:c.1767_1769del	XP_011518255.1:p.Cys589_Leu590delinsTrp
XR_242782.2:n.3851_3853del
XR_930851.1:n.3828+23_3828+25del
NM_001348749.1:c.3597_3599del	NP_001335678.1:p.Cys1199_Leu1200delinsTrp
NM_001348750.1:c.3381_3383del	NP_001335679.1:p.Cys1127_Leu1128delinsTrp
NR_145966.2:n.3843_3845del
NM_015213.4:c.3669_3671del MANE Select	NP_056028.2:p.Cys1223_Leu1224delinsTrp
NM_001243254.2:c.3646+23_3646+25del	NP_001230183.1:n.3646+23_3646+25del
NM_001348749.2:c.3597_3599del	NP_001335678.1:p.Cys1199_Leu1200delinsTrp
NM_001348750.2:c.3381_3383del	NP_001335679.1:p.Cys1127_Leu1128delinsTrp