Canonical Allele Identifier: CA2612398833

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9141828-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141828C>A , CM000673.2:g.9141828C>A	GRCh38
NC_000011.9:g.9163375C>A , CM000673.1:g.9163375C>A	GRCh37
NC_000011.8:g.9119951C>A	NCBI36
NG_053019.1:g.128508G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+112G>T MANE Select	ENSP00000328524.3:n.3680+112G>T
ENST00000525784.6:n.1542+112G>T
ENST00000530780.2:c.*3506+112G>T	ENSP00000433925.1:n.*3506+112G>T
ENST00000531747.2:n.3351+112G>T
ENST00000679446.1:n.3713G>T
ENST00000679458.1:n.5081+112G>T
ENST00000679460.1:n.4742+112G>T
ENST00000679568.1:c.3680+112G>T	ENSP00000505860.1:n.3680+112G>T
ENST00000679745.1:n.4185+112G>T
ENST00000679773.1:n.2841+112G>T
ENST00000679926.1:n.4982+112G>T
ENST00000679999.1:c.*737+112G>T	ENSP00000505198.1:n.*737+112G>T
ENST00000680252.1:c.3347+112G>T
ENST00000680294.1:c.3473+112G>T	ENSP00000506113.1:n.3473+112G>T
ENST00000680358.1:n.2979+112G>T
ENST00000680470.1:c.*1461+112G>T	ENSP00000505975.1:n.*1461+112G>T
ENST00000680554.1:c.*213+112G>T	ENSP00000505621.1:n.*213+112G>T
ENST00000680576.1:n.5268G>T
ENST00000680599.1:n.3721+112G>T
ENST00000680742.1:c.*179+146G>T	ENSP00000505206.1:n.*179+146G>T
ENST00000680791.1:n.2564+112G>T
ENST00000680885.1:n.5382+112G>T
ENST00000681158.1:c.3264+112G>T
ENST00000681203.1:c.3608+112G>T	ENSP00000506456.1:n.3608+112G>T
ENST00000681371.1:n.3552+112G>T
ENST00000681425.1:n.4158+112G>T
ENST00000681639.1:n.1959+112G>T
ENST00000328194.7:c.3680+112G>T	ENSP00000328524.3:n.3680+112G>T
ENST00000525784.5:c.616+112G>T
ENST00000527700.5:n.3242+112G>T
ENST00000528725.5:c.376+112G>T
ENST00000529977.5:n.1581+112G>T
ENST00000530044.5:c.3646+146G>T	ENSP00000435866.1:n.3646+146G>T
ENST00000533737.5:c.343+112G>T
NM_001243254.1:c.3646+146G>T	NP_001230183.1:n.3646+146G>T
NM_015213.3:c.3680+112G>T	NP_056028.2:n.3680+112G>T
XM_005252832.1:c.3680+112G>T	XP_005252889.1:n.3680+112G>T
XM_011519952.1:c.3646+146G>T	XP_011518254.1:n.3646+146G>T
XM_011519953.1:c.1778+112G>T	XP_011518255.1:n.1778+112G>T
XR_242782.2:n.3862+112G>T
XR_930851.1:n.3828+146G>T
NM_001348749.1:c.3608+112G>T	NP_001335678.1:n.3608+112G>T
NM_001348750.1:c.3392+112G>T	NP_001335679.1:n.3392+112G>T
NR_145966.2:n.3854+112G>T
NM_015213.4:c.3680+112G>T MANE Select	NP_056028.2:n.3680+112G>T
NM_001243254.2:c.3646+146G>T	NP_001230183.1:n.3646+146G>T
NM_001348749.2:c.3608+112G>T	NP_001335678.1:n.3608+112G>T
NM_001348750.2:c.3392+112G>T	NP_001335679.1:n.3392+112G>T