Canonical Allele Identifier: CA2612401176

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9160703-C-CGT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160703_9160704insGT , CM000673.2:g.9160703_9160704insGT	GRCh38
NC_000011.9:g.9182250_9182251insGT , CM000673.1:g.9182250_9182251insGT	GRCh37
NC_000011.8:g.9138826_9138827insGT	NCBI36
NG_053019.1:g.109632_109633insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2436+9_2436+10insAC MANE Select	ENSP00000328524.3:n.2436+9_2436+10insAC
ENST00000530780.2:c.*2262+9_*2262+10insAC	ENSP00000433925.1:n.*2262+9_*2262+10insAC
ENST00000679446.1:n.2357+9_2357+10insAC
ENST00000679458.1:n.3837+9_3837+10insAC
ENST00000679460.1:n.2225+9_2225+10insAC
ENST00000679568.1:c.2436+9_2436+10insAC	ENSP00000505860.1:n.2436+9_2436+10insAC
ENST00000679745.1:n.2225+9_2225+10insAC
ENST00000679926.1:n.1252+9_1252+10insAC
ENST00000679999.1:c.2436+9_2436+10insAC	ENSP00000505198.1:n.2436+9_2436+10insAC
ENST00000680252.1:c.2225+9_2225+10insAC
ENST00000680294.1:c.2436+9_2436+10insAC	ENSP00000506113.1:n.2436+9_2436+10insAC
ENST00000680358.1:n.1735+9_1735+10insAC
ENST00000680470.1:c.*302+9_*302+10insAC	ENSP00000505975.1:n.*302+9_*302+10insAC
ENST00000680554.1:c.2148+9_2148+10insAC	ENSP00000505621.1:n.2148+9_2148+10insAC
ENST00000680576.1:n.2225+9_2225+10insAC
ENST00000680599.1:n.2353+9_2353+10insAC
ENST00000680742.1:c.2436+9_2436+10insAC	ENSP00000505206.1:n.2436+9_2436+10insAC
ENST00000680885.1:n.2357+9_2357+10insAC
ENST00000681158.1:c.2225+9_2225+10insAC
ENST00000681173.1:n.2225+9_2225+10insAC
ENST00000681203.1:c.2364+9_2364+10insAC	ENSP00000506456.1:n.2364+9_2364+10insAC
ENST00000681425.1:n.2357+9_2357+10insAC
ENST00000328194.7:c.2436+9_2436+10insAC	ENSP00000328524.3:n.2436+9_2436+10insAC
ENST00000526707.5:c.2364+9_2364+10insAC	ENSP00000436780.1:n.2364+9_2364+10insAC
ENST00000527700.5:n.1998+9_1998+10insAC
ENST00000530044.5:c.2436+9_2436+10insAC	ENSP00000435866.1:n.2436+9_2436+10insAC
NM_001243254.1:c.2436+9_2436+10insAC	NP_001230183.1:n.2436+9_2436+10insAC
NM_015213.3:c.2436+9_2436+10insAC	NP_056028.2:n.2436+9_2436+10insAC
XM_005252832.1:c.2436+9_2436+10insAC	XP_005252889.1:n.2436+9_2436+10insAC
XM_011519952.1:c.2436+9_2436+10insAC	XP_011518254.1:n.2436+9_2436+10insAC
XM_011519953.1:c.534+9_534+10insAC	XP_011518255.1:n.534+9_534+10insAC
XR_242782.2:n.2701+9_2701+10insAC
XR_930851.1:n.2701+9_2701+10insAC
XR_930852.1:n.2701+9_2701+10insAC
XR_930853.1:n.2550+9_2550+10insAC
NM_001348749.1:c.2364+9_2364+10insAC	NP_001335678.1:n.2364+9_2364+10insAC
NM_001348750.1:c.2148+9_2148+10insAC	NP_001335679.1:n.2148+9_2148+10insAC
NR_145966.2:n.2693+9_2693+10insAC
NM_015213.4:c.2436+9_2436+10insAC MANE Select	NP_056028.2:n.2436+9_2436+10insAC
NM_001243254.2:c.2436+9_2436+10insAC	NP_001230183.1:n.2436+9_2436+10insAC
NM_001348749.2:c.2364+9_2364+10insAC	NP_001335678.1:n.2364+9_2364+10insAC
NM_001348750.2:c.2148+9_2148+10insAC	NP_001335679.1:n.2148+9_2148+10insAC