Canonical Allele Identifier: CA1951464283

Gene: DENND5A

Linked Data

• dbSNP Id: rs1847949368

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160680_9160691dup , CM000673.2:g.9160680_9160691dup	GRCh38
NC_000011.9:g.9182227_9182238dup , CM000673.1:g.9182227_9182238dup	GRCh37
NC_000011.8:g.9138803_9138814dup	NCBI36
NG_053019.1:g.109649_109660dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2436+26_2436+37dup MANE Select	ENSP00000328524.3:n.2436+26_2436+37dup
ENST00000530780.2:c.*2262+26_*2262+37dup	ENSP00000433925.1:n.*2262+26_*2262+37dup
ENST00000679446.1:n.2357+26_2357+37dup
ENST00000679458.1:n.3837+26_3837+37dup
ENST00000679460.1:n.2225+26_2225+37dup
ENST00000679568.1:c.2436+26_2436+37dup	ENSP00000505860.1:n.2436+26_2436+37dup
ENST00000679745.1:n.2225+26_2225+37dup
ENST00000679926.1:n.1252+26_1252+37dup
ENST00000679999.1:c.2436+26_2436+37dup	ENSP00000505198.1:n.2436+26_2436+37dup
ENST00000680252.1:c.2225+26_2225+37dup
ENST00000680294.1:c.2436+26_2436+37dup	ENSP00000506113.1:n.2436+26_2436+37dup
ENST00000680358.1:n.1735+26_1735+37dup
ENST00000680470.1:c.*302+26_*302+37dup	ENSP00000505975.1:n.*302+26_*302+37dup
ENST00000680554.1:c.2148+26_2148+37dup	ENSP00000505621.1:n.2148+26_2148+37dup
ENST00000680576.1:n.2225+26_2225+37dup
ENST00000680599.1:n.2353+26_2353+37dup
ENST00000680742.1:c.2436+26_2436+37dup	ENSP00000505206.1:n.2436+26_2436+37dup
ENST00000680885.1:n.2357+26_2357+37dup
ENST00000681158.1:c.2225+26_2225+37dup
ENST00000681173.1:n.2225+26_2225+37dup
ENST00000681203.1:c.2364+26_2364+37dup	ENSP00000506456.1:n.2364+26_2364+37dup
ENST00000681425.1:n.2357+26_2357+37dup
ENST00000328194.7:c.2436+26_2436+37dup	ENSP00000328524.3:n.2436+26_2436+37dup
ENST00000526707.5:c.2364+26_2364+37dup	ENSP00000436780.1:n.2364+26_2364+37dup
ENST00000527700.5:n.1998+26_1998+37dup
ENST00000530044.5:c.2436+26_2436+37dup	ENSP00000435866.1:n.2436+26_2436+37dup
NM_001243254.1:c.2436+26_2436+37dup	NP_001230183.1:n.2436+26_2436+37dup
NM_015213.3:c.2436+26_2436+37dup	NP_056028.2:n.2436+26_2436+37dup
XM_005252832.1:c.2436+26_2436+37dup	XP_005252889.1:n.2436+26_2436+37dup
XM_011519952.1:c.2436+26_2436+37dup	XP_011518254.1:n.2436+26_2436+37dup
XM_011519953.1:c.534+26_534+37dup	XP_011518255.1:n.534+26_534+37dup
XR_242782.2:n.2701+26_2701+37dup
XR_930851.1:n.2701+26_2701+37dup
XR_930852.1:n.2701+26_2701+37dup
XR_930853.1:n.2550+26_2550+37dup
NM_001348749.1:c.2364+26_2364+37dup	NP_001335678.1:n.2364+26_2364+37dup
NM_001348750.1:c.2148+26_2148+37dup	NP_001335679.1:n.2148+26_2148+37dup
NR_145966.2:n.2693+26_2693+37dup
NM_015213.4:c.2436+26_2436+37dup MANE Select	NP_056028.2:n.2436+26_2436+37dup
NM_001243254.2:c.2436+26_2436+37dup	NP_001230183.1:n.2436+26_2436+37dup
NM_001348749.2:c.2364+26_2364+37dup	NP_001335678.1:n.2364+26_2364+37dup
NM_001348750.2:c.2148+26_2148+37dup	NP_001335679.1:n.2148+26_2148+37dup