Canonical Allele Identifier: CA2612398790

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9141801-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141801G>T , CM000673.2:g.9141801G>T	GRCh38
NC_000011.9:g.9163348G>T , CM000673.1:g.9163348G>T	GRCh37
NC_000011.8:g.9119924G>T	NCBI36
NG_053019.1:g.128535C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+139C>A MANE Select	ENSP00000328524.3:n.3680+139C>A
ENST00000525784.6:n.1542+139C>A
ENST00000530780.2:c.*3506+139C>A	ENSP00000433925.1:n.*3506+139C>A
ENST00000531747.2:n.3351+139C>A
ENST00000679446.1:n.3740C>A
ENST00000679458.1:n.5081+139C>A
ENST00000679460.1:n.4742+139C>A
ENST00000679568.1:c.3680+139C>A	ENSP00000505860.1:n.3680+139C>A
ENST00000679745.1:n.4185+139C>A
ENST00000679773.1:n.2841+139C>A
ENST00000679926.1:n.4982+139C>A
ENST00000679999.1:c.*737+139C>A	ENSP00000505198.1:n.*737+139C>A
ENST00000680252.1:c.3347+139C>A
ENST00000680294.1:c.3473+139C>A	ENSP00000506113.1:n.3473+139C>A
ENST00000680358.1:n.2979+139C>A
ENST00000680470.1:c.*1461+139C>A	ENSP00000505975.1:n.*1461+139C>A
ENST00000680554.1:c.*213+139C>A	ENSP00000505621.1:n.*213+139C>A
ENST00000680576.1:n.5295C>A
ENST00000680599.1:n.3721+139C>A
ENST00000680742.1:c.*179+173C>A	ENSP00000505206.1:n.*179+173C>A
ENST00000680791.1:n.2564+139C>A
ENST00000680885.1:n.5382+139C>A
ENST00000681158.1:c.3264+139C>A
ENST00000681203.1:c.3608+139C>A	ENSP00000506456.1:n.3608+139C>A
ENST00000681371.1:n.3552+139C>A
ENST00000681425.1:n.4158+139C>A
ENST00000681639.1:n.1959+139C>A
ENST00000328194.7:c.3680+139C>A	ENSP00000328524.3:n.3680+139C>A
ENST00000525784.5:c.616+139C>A
ENST00000527700.5:n.3242+139C>A
ENST00000528725.5:c.376+139C>A
ENST00000529977.5:n.1581+139C>A
ENST00000530044.5:c.3646+173C>A	ENSP00000435866.1:n.3646+173C>A
ENST00000533737.5:c.343+139C>A
NM_001243254.1:c.3646+173C>A	NP_001230183.1:n.3646+173C>A
NM_015213.3:c.3680+139C>A	NP_056028.2:n.3680+139C>A
XM_005252832.1:c.3680+139C>A	XP_005252889.1:n.3680+139C>A
XM_011519952.1:c.3646+173C>A	XP_011518254.1:n.3646+173C>A
XM_011519953.1:c.1778+139C>A	XP_011518255.1:n.1778+139C>A
XR_242782.2:n.3862+139C>A
XR_930851.1:n.3828+173C>A
NM_001348749.1:c.3608+139C>A	NP_001335678.1:n.3608+139C>A
NM_001348750.1:c.3392+139C>A	NP_001335679.1:n.3392+139C>A
NR_145966.2:n.3854+139C>A
NM_015213.4:c.3680+139C>A MANE Select	NP_056028.2:n.3680+139C>A
NM_001243254.2:c.3646+173C>A	NP_001230183.1:n.3646+173C>A
NM_001348749.2:c.3608+139C>A	NP_001335678.1:n.3608+139C>A
NM_001348750.2:c.3392+139C>A	NP_001335679.1:n.3392+139C>A