Canonical Allele Identifier: CA645584004

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9160842-CT-C
• COSMIC: COSM5839786

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160846del , CM000673.2:g.9160846del	GRCh38
NC_000011.9:g.9182393del , CM000673.1:g.9182393del	GRCh37
NC_000011.8:g.9138969del	NCBI36
NG_053019.1:g.109493del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2306del MANE Select	ENSP00000328524.3:p.Lys769ArgfsTer9
ENST00000530780.2:c.*2132del	ENSP00000433925.1:n.*2132del
ENST00000679446.1:n.2227del
ENST00000679458.1:n.3707del
ENST00000679460.1:n.2095del
ENST00000679568.1:c.2306del	ENSP00000505860.1:p.Lys769ArgfsTer9
ENST00000679745.1:n.2095del
ENST00000679926.1:n.1122del
ENST00000679999.1:c.2306del	ENSP00000505198.1:p.Lys769ArgfsTer9
ENST00000680252.1:c.2095del
ENST00000680294.1:c.2306del	ENSP00000506113.1:p.Lys769ArgfsTer9
ENST00000680358.1:n.1605del
ENST00000680470.1:c.*172del	ENSP00000505975.1:n.*172del
ENST00000680554.1:c.2018del	ENSP00000505621.1:p.Lys673ArgfsTer9
ENST00000680576.1:n.2095del
ENST00000680599.1:n.2223del
ENST00000680742.1:c.2306del	ENSP00000505206.1:p.Lys769ArgfsTer9
ENST00000680885.1:n.2227del
ENST00000681158.1:c.2095del
ENST00000681173.1:n.2095del
ENST00000681203.1:c.2234del	ENSP00000506456.1:p.Lys745ArgfsTer9
ENST00000681425.1:n.2227del
ENST00000328194.7:c.2306del	ENSP00000328524.3:p.Lys769ArgfsTer9
ENST00000526707.5:c.2234del	ENSP00000436780.1:p.Lys745ArgfsTer9
ENST00000527700.5:n.1868del
ENST00000530044.5:c.2306del	ENSP00000435866.1:p.Lys769ArgfsTer9
NM_001243254.1:c.2306del	NP_001230183.1:p.Lys769ArgfsTer9
NM_015213.3:c.2306del	NP_056028.2:p.Lys769ArgfsTer9
XM_005252832.1:c.2306del	XP_005252889.1:p.Lys769ArgfsTer9
XM_011519952.1:c.2306del	XP_011518254.1:p.Lys769ArgfsTer9
XM_011519953.1:c.404del	XP_011518255.1:p.Lys135ArgfsTer9
XR_242782.2:n.2571del
XR_930851.1:n.2571del
XR_930852.1:n.2571del
XR_930853.1:n.2420del
NM_001348749.1:c.2234del	NP_001335678.1:p.Lys745ArgfsTer9
NM_001348750.1:c.2018del	NP_001335679.1:p.Lys673ArgfsTer9
NR_145966.2:n.2563del
NM_015213.4:c.2306del MANE Select	NP_056028.2:p.Lys769ArgfsTer9
NM_001243254.2:c.2306del	NP_001230183.1:p.Lys769ArgfsTer9
NM_001348749.2:c.2234del	NP_001335678.1:p.Lys745ArgfsTer9
NM_001348750.2:c.2018del	NP_001335679.1:p.Lys673ArgfsTer9