Canonical Allele Identifier: CA1951453966

Gene: DENND5A

Linked Data

• dbSNP Id: rs1847250903

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141818_9141820del , CM000673.2:g.9141818_9141820del	GRCh38
NC_000011.9:g.9163365_9163367del , CM000673.1:g.9163365_9163367del	GRCh37
NC_000011.8:g.9119941_9119943del	NCBI36
NG_053019.1:g.128518_128520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+122_3680+124del MANE Select	ENSP00000328524.3:n.3680+122_3680+124del
ENST00000525784.6:n.1542+122_1542+124del
ENST00000530780.2:c.*3506+122_*3506+124del	ENSP00000433925.1:n.*3506+122_*3506+124del
ENST00000531747.2:n.3351+122_3351+124del
ENST00000679446.1:n.3723_3725del
ENST00000679458.1:n.5081+122_5081+124del
ENST00000679460.1:n.4742+122_4742+124del
ENST00000679568.1:c.3680+122_3680+124del	ENSP00000505860.1:n.3680+122_3680+124del
ENST00000679745.1:n.4185+122_4185+124del
ENST00000679773.1:n.2841+122_2841+124del
ENST00000679926.1:n.4982+122_4982+124del
ENST00000679999.1:c.*737+122_*737+124del	ENSP00000505198.1:n.*737+122_*737+124del
ENST00000680252.1:c.3347+122_3347+124del
ENST00000680294.1:c.3473+122_3473+124del	ENSP00000506113.1:n.3473+122_3473+124del
ENST00000680358.1:n.2979+122_2979+124del
ENST00000680470.1:c.*1461+122_*1461+124del	ENSP00000505975.1:n.*1461+122_*1461+124del
ENST00000680554.1:c.*213+122_*213+124del	ENSP00000505621.1:n.*213+122_*213+124del
ENST00000680576.1:n.5278_5280del
ENST00000680599.1:n.3721+122_3721+124del
ENST00000680742.1:c.*179+156_*179+158del	ENSP00000505206.1:n.*179+156_*179+158del
ENST00000680791.1:n.2564+122_2564+124del
ENST00000680885.1:n.5382+122_5382+124del
ENST00000681158.1:c.3264+122_3264+124del
ENST00000681203.1:c.3608+122_3608+124del	ENSP00000506456.1:n.3608+122_3608+124del
ENST00000681371.1:n.3552+122_3552+124del
ENST00000681425.1:n.4158+122_4158+124del
ENST00000681639.1:n.1959+122_1959+124del
ENST00000328194.7:c.3680+122_3680+124del	ENSP00000328524.3:n.3680+122_3680+124del
ENST00000525784.5:c.616+122_616+124del
ENST00000527700.5:n.3242+122_3242+124del
ENST00000528725.5:c.376+122_376+124del
ENST00000529977.5:n.1581+122_1581+124del
ENST00000530044.5:c.3646+156_3646+158del	ENSP00000435866.1:n.3646+156_3646+158del
ENST00000533737.5:c.343+122_343+124del
NM_001243254.1:c.3646+156_3646+158del	NP_001230183.1:n.3646+156_3646+158del
NM_015213.3:c.3680+122_3680+124del	NP_056028.2:n.3680+122_3680+124del
XM_005252832.1:c.3680+122_3680+124del	XP_005252889.1:n.3680+122_3680+124del
XM_011519952.1:c.3646+156_3646+158del	XP_011518254.1:n.3646+156_3646+158del
XM_011519953.1:c.1778+122_1778+124del	XP_011518255.1:n.1778+122_1778+124del
XR_242782.2:n.3862+122_3862+124del
XR_930851.1:n.3828+156_3828+158del
NM_001348749.1:c.3608+122_3608+124del	NP_001335678.1:n.3608+122_3608+124del
NM_001348750.1:c.3392+122_3392+124del	NP_001335679.1:n.3392+122_3392+124del
NR_145966.2:n.3854+122_3854+124del
NM_015213.4:c.3680+122_3680+124del MANE Select	NP_056028.2:n.3680+122_3680+124del
NM_001243254.2:c.3646+156_3646+158del	NP_001230183.1:n.3646+156_3646+158del
NM_001348749.2:c.3608+122_3608+124del	NP_001335678.1:n.3608+122_3608+124del
NM_001348750.2:c.3392+122_3392+124del	NP_001335679.1:n.3392+122_3392+124del