Canonical Allele Identifier: CA681757748

Gene: DENND5A

Linked Data

• dbSNP Id: rs1191692451
• MyVariant Identifiers: chr11:g.9163332_9163333del (hg19) ; chr11:g.9141785_9141786del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141788_9141789del , CM000673.2:g.9141788_9141789del	GRCh38
NC_000011.9:g.9163335_9163336del , CM000673.1:g.9163335_9163336del	GRCh37
NC_000011.8:g.9119911_9119912del	NCBI36
NG_053019.1:g.128550_128551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+154_3680+155del MANE Select	ENSP00000328524.3:n.3680+154_3680+155del
ENST00000525784.6:n.1542+154_1542+155del
ENST00000530780.2:c.*3506+154_*3506+155del	ENSP00000433925.1:n.*3506+154_*3506+155del
ENST00000531747.2:n.3351+154_3351+155del
ENST00000679446.1:n.3755_3756del
ENST00000679458.1:n.5081+154_5081+155del
ENST00000679460.1:n.4742+154_4742+155del
ENST00000679568.1:c.3680+154_3680+155del	ENSP00000505860.1:n.3680+154_3680+155del
ENST00000679745.1:n.4185+154_4185+155del
ENST00000679773.1:n.2841+154_2841+155del
ENST00000679926.1:n.4982+154_4982+155del
ENST00000679999.1:c.*737+154_*737+155del	ENSP00000505198.1:n.*737+154_*737+155del
ENST00000680252.1:c.3347+154_3347+155del
ENST00000680294.1:c.3473+154_3473+155del	ENSP00000506113.1:n.3473+154_3473+155del
ENST00000680358.1:n.2979+154_2979+155del
ENST00000680470.1:c.*1461+154_*1461+155del	ENSP00000505975.1:n.*1461+154_*1461+155del
ENST00000680554.1:c.*213+154_*213+155del	ENSP00000505621.1:n.*213+154_*213+155del
ENST00000680576.1:n.5310_5311del
ENST00000680599.1:n.3721+154_3721+155del
ENST00000680742.1:c.*179+188_*179+189del	ENSP00000505206.1:n.*179+188_*179+189del
ENST00000680791.1:n.2564+154_2564+155del
ENST00000680885.1:n.5382+154_5382+155del
ENST00000681158.1:c.3264+154_3264+155del
ENST00000681203.1:c.3608+154_3608+155del	ENSP00000506456.1:n.3608+154_3608+155del
ENST00000681371.1:n.3552+154_3552+155del
ENST00000681425.1:n.4158+154_4158+155del
ENST00000681639.1:n.1959+154_1959+155del
ENST00000328194.7:c.3680+154_3680+155del	ENSP00000328524.3:n.3680+154_3680+155del
ENST00000525784.5:c.616+154_616+155del
ENST00000527700.5:n.3242+154_3242+155del
ENST00000528725.5:c.376+154_376+155del
ENST00000529977.5:n.1581+154_1581+155del
ENST00000530044.5:c.3646+188_3646+189del	ENSP00000435866.1:n.3646+188_3646+189del
ENST00000533737.5:c.343+154_343+155del
NM_001243254.1:c.3646+188_3646+189del	NP_001230183.1:n.3646+188_3646+189del
NM_015213.3:c.3680+154_3680+155del	NP_056028.2:n.3680+154_3680+155del
XM_005252832.1:c.3680+154_3680+155del	XP_005252889.1:n.3680+154_3680+155del
XM_011519952.1:c.3646+188_3646+189del	XP_011518254.1:n.3646+188_3646+189del
XM_011519953.1:c.1778+154_1778+155del	XP_011518255.1:n.1778+154_1778+155del
XR_242782.2:n.3862+154_3862+155del
XR_930851.1:n.3828+188_3828+189del
NM_001348749.1:c.3608+154_3608+155del	NP_001335678.1:n.3608+154_3608+155del
NM_001348750.1:c.3392+154_3392+155del	NP_001335679.1:n.3392+154_3392+155del
NR_145966.2:n.3854+154_3854+155del
NM_015213.4:c.3680+154_3680+155del MANE Select	NP_056028.2:n.3680+154_3680+155del
NM_001243254.2:c.3646+188_3646+189del	NP_001230183.1:n.3646+188_3646+189del
NM_001348749.2:c.3608+154_3608+155del	NP_001335678.1:n.3608+154_3608+155del
NM_001348750.2:c.3392+154_3392+155del	NP_001335679.1:n.3392+154_3392+155del