Canonical Allele Identifier: CA681769750

Gene: DENND5A

Linked Data

• dbSNP Id: rs1458739521
• MyVariant Identifiers: chr11:g.9182045_9182059del (hg19) ; chr11:g.9160498_9160512del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160498_9160512del , CM000673.2:g.9160498_9160512del	GRCh38
NC_000011.9:g.9182045_9182059del , CM000673.1:g.9182045_9182059del	GRCh37
NC_000011.8:g.9138621_9138635del	NCBI36
NG_053019.1:g.109824_109838del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2436+201_2436+215del MANE Select	ENSP00000328524.3:n.2436+201_2436+215del
ENST00000530780.2:c.*2262+201_*2262+215del	ENSP00000433925.1:n.*2262+201_*2262+215del
ENST00000679446.1:n.2357+201_2357+215del
ENST00000679458.1:n.3837+201_3837+215del
ENST00000679460.1:n.2225+201_2225+215del
ENST00000679568.1:c.2436+201_2436+215del	ENSP00000505860.1:n.2436+201_2436+215del
ENST00000679745.1:n.2225+201_2225+215del
ENST00000679926.1:n.1252+201_1252+215del
ENST00000679999.1:c.2436+201_2436+215del	ENSP00000505198.1:n.2436+201_2436+215del
ENST00000680252.1:c.2225+201_2225+215del
ENST00000680294.1:c.2436+201_2436+215del	ENSP00000506113.1:n.2436+201_2436+215del
ENST00000680358.1:n.1735+201_1735+215del
ENST00000680470.1:c.*302+201_*302+215del	ENSP00000505975.1:n.*302+201_*302+215del
ENST00000680554.1:c.2148+201_2148+215del	ENSP00000505621.1:n.2148+201_2148+215del
ENST00000680576.1:n.2225+201_2225+215del
ENST00000680599.1:n.2353+201_2353+215del
ENST00000680742.1:c.2436+201_2436+215del	ENSP00000505206.1:n.2436+201_2436+215del
ENST00000680885.1:n.2357+201_2357+215del
ENST00000681158.1:c.2225+201_2225+215del
ENST00000681173.1:n.2225+201_2226-199del
ENST00000681203.1:c.2364+201_2364+215del	ENSP00000506456.1:n.2364+201_2364+215del
ENST00000681425.1:n.2357+201_2357+215del
ENST00000328194.7:c.2436+201_2436+215del	ENSP00000328524.3:n.2436+201_2436+215del
ENST00000526707.5:c.2364+201_2364+215del	ENSP00000436780.1:n.2364+201_2364+215del
ENST00000527700.5:n.1998+201_1998+215del
ENST00000530044.5:c.2436+201_2436+215del	ENSP00000435866.1:n.2436+201_2436+215del
NM_001243254.1:c.2436+201_2436+215del	NP_001230183.1:n.2436+201_2436+215del
NM_015213.3:c.2436+201_2436+215del	NP_056028.2:n.2436+201_2436+215del
XM_005252832.1:c.2436+201_2436+215del	XP_005252889.1:n.2436+201_2436+215del
XM_011519952.1:c.2436+201_2436+215del	XP_011518254.1:n.2436+201_2436+215del
XM_011519953.1:c.534+201_534+215del	XP_011518255.1:n.534+201_534+215del
XR_242782.2:n.2701+201_2701+215del
XR_930851.1:n.2701+201_2701+215del
XR_930852.1:n.2701+201_2701+215del
XR_930853.1:n.2550+201_2550+215del
NM_001348749.1:c.2364+201_2364+215del	NP_001335678.1:n.2364+201_2364+215del
NM_001348750.1:c.2148+201_2148+215del	NP_001335679.1:n.2148+201_2148+215del
NR_145966.2:n.2693+201_2693+215del
NM_015213.4:c.2436+201_2436+215del MANE Select	NP_056028.2:n.2436+201_2436+215del
NM_001243254.2:c.2436+201_2436+215del	NP_001230183.1:n.2436+201_2436+215del
NM_001348749.2:c.2364+201_2364+215del	NP_001335678.1:n.2364+201_2364+215del
NM_001348750.2:c.2148+201_2148+215del	NP_001335679.1:n.2148+201_2148+215del