Canonical Allele Identifier: CA2574750104

Gene: DENND5A

Linked Data

• dbSNP Id: rs2136109826
• gnomAD v4: 11-9141864-CCCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141866_9141869del , CM000673.2:g.9141866_9141869del	GRCh38
NC_000011.9:g.9163413_9163416del , CM000673.1:g.9163413_9163416del	GRCh37
NC_000011.8:g.9119989_9119992del	NCBI36
NG_053019.1:g.128468_128471del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+72_3680+75del MANE Select	ENSP00000328524.3:n.3680+72_3680+75del
ENST00000525784.6:n.1542+72_1542+75del
ENST00000530780.2:c.*3506+72_*3506+75del	ENSP00000433925.1:n.*3506+72_*3506+75del
ENST00000531747.2:n.3351+72_3351+75del
ENST00000679446.1:n.3673_3676del
ENST00000679458.1:n.5081+72_5081+75del
ENST00000679460.1:n.4742+72_4742+75del
ENST00000679568.1:c.3680+72_3680+75del	ENSP00000505860.1:n.3680+72_3680+75del
ENST00000679745.1:n.4185+72_4185+75del
ENST00000679773.1:n.2841+72_2841+75del
ENST00000679926.1:n.4982+72_4982+75del
ENST00000679999.1:c.*737+72_*737+75del	ENSP00000505198.1:n.*737+72_*737+75del
ENST00000680252.1:c.3347+72_3347+75del
ENST00000680294.1:c.3473+72_3473+75del	ENSP00000506113.1:n.3473+72_3473+75del
ENST00000680358.1:n.2979+72_2979+75del
ENST00000680470.1:c.*1461+72_*1461+75del	ENSP00000505975.1:n.*1461+72_*1461+75del
ENST00000680554.1:c.*213+72_*213+75del	ENSP00000505621.1:n.*213+72_*213+75del
ENST00000680576.1:n.5228_5231del
ENST00000680599.1:n.3721+72_3721+75del
ENST00000680742.1:c.*179+106_*179+109del	ENSP00000505206.1:n.*179+106_*179+109del
ENST00000680791.1:n.2564+72_2564+75del
ENST00000680885.1:n.5382+72_5382+75del
ENST00000681158.1:c.3264+72_3264+75del
ENST00000681203.1:c.3608+72_3608+75del	ENSP00000506456.1:n.3608+72_3608+75del
ENST00000681371.1:n.3552+72_3552+75del
ENST00000681425.1:n.4158+72_4158+75del
ENST00000681639.1:n.1959+72_1959+75del
ENST00000328194.7:c.3680+72_3680+75del	ENSP00000328524.3:n.3680+72_3680+75del
ENST00000525784.5:c.616+72_616+75del
ENST00000527700.5:n.3242+72_3242+75del
ENST00000528725.5:c.376+72_376+75del
ENST00000529977.5:n.1581+72_1581+75del
ENST00000530044.5:c.3646+106_3646+109del	ENSP00000435866.1:n.3646+106_3646+109del
ENST00000533737.5:c.343+72_343+75del
NM_001243254.1:c.3646+106_3646+109del	NP_001230183.1:n.3646+106_3646+109del
NM_015213.3:c.3680+72_3680+75del	NP_056028.2:n.3680+72_3680+75del
XM_005252832.1:c.3680+72_3680+75del	XP_005252889.1:n.3680+72_3680+75del
XM_011519952.1:c.3646+106_3646+109del	XP_011518254.1:n.3646+106_3646+109del
XM_011519953.1:c.1778+72_1778+75del	XP_011518255.1:n.1778+72_1778+75del
XR_242782.2:n.3862+72_3862+75del
XR_930851.1:n.3828+106_3828+109del
NM_001348749.1:c.3608+72_3608+75del	NP_001335678.1:n.3608+72_3608+75del
NM_001348750.1:c.3392+72_3392+75del	NP_001335679.1:n.3392+72_3392+75del
NR_145966.2:n.3854+72_3854+75del
NM_015213.4:c.3680+72_3680+75del MANE Select	NP_056028.2:n.3680+72_3680+75del
NM_001243254.2:c.3646+106_3646+109del	NP_001230183.1:n.3646+106_3646+109del
NM_001348749.2:c.3608+72_3608+75del	NP_001335678.1:n.3608+72_3608+75del
NM_001348750.2:c.3392+72_3392+75del	NP_001335679.1:n.3392+72_3392+75del