Canonical Allele Identifier: CA1951454021

Gene: DENND5A

Linked Data

• dbSNP Id: rs1847254787

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141893C>T , CM000673.2:g.9141893C>T	GRCh38
NC_000011.9:g.9163440C>T , CM000673.1:g.9163440C>T	GRCh37
NC_000011.8:g.9120016C>T	NCBI36
NG_053019.1:g.128443G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3680+47G>A MANE Select	ENSP00000328524.3:n.3680+47G>A
ENST00000525784.6:n.1542+47G>A
ENST00000530780.2:c.*3506+47G>A	ENSP00000433925.1:n.*3506+47G>A
ENST00000531747.2:n.3351+47G>A
ENST00000679446.1:n.3648G>A
ENST00000679458.1:n.5081+47G>A
ENST00000679460.1:n.4742+47G>A
ENST00000679568.1:c.3680+47G>A	ENSP00000505860.1:n.3680+47G>A
ENST00000679745.1:n.4185+47G>A
ENST00000679773.1:n.2841+47G>A
ENST00000679926.1:n.4982+47G>A
ENST00000679999.1:c.*737+47G>A	ENSP00000505198.1:n.*737+47G>A
ENST00000680252.1:c.3347+47G>A
ENST00000680294.1:c.3473+47G>A	ENSP00000506113.1:n.3473+47G>A
ENST00000680358.1:n.2979+47G>A
ENST00000680470.1:c.*1461+47G>A	ENSP00000505975.1:n.*1461+47G>A
ENST00000680554.1:c.*213+47G>A	ENSP00000505621.1:n.*213+47G>A
ENST00000680576.1:n.5203G>A
ENST00000680599.1:n.3721+47G>A
ENST00000680742.1:c.*179+81G>A	ENSP00000505206.1:n.*179+81G>A
ENST00000680791.1:n.2564+47G>A
ENST00000680885.1:n.5382+47G>A
ENST00000681158.1:c.3264+47G>A
ENST00000681203.1:c.3608+47G>A	ENSP00000506456.1:n.3608+47G>A
ENST00000681371.1:n.3552+47G>A
ENST00000681425.1:n.4158+47G>A
ENST00000681639.1:n.1959+47G>A
ENST00000328194.7:c.3680+47G>A	ENSP00000328524.3:n.3680+47G>A
ENST00000525784.5:c.616+47G>A
ENST00000527700.5:n.3242+47G>A
ENST00000528725.5:c.376+47G>A
ENST00000529977.5:n.1581+47G>A
ENST00000530044.5:c.3646+81G>A	ENSP00000435866.1:n.3646+81G>A
ENST00000533737.5:c.343+47G>A
NM_001243254.1:c.3646+81G>A	NP_001230183.1:n.3646+81G>A
NM_015213.3:c.3680+47G>A	NP_056028.2:n.3680+47G>A
XM_005252832.1:c.3680+47G>A	XP_005252889.1:n.3680+47G>A
XM_011519952.1:c.3646+81G>A	XP_011518254.1:n.3646+81G>A
XM_011519953.1:c.1778+47G>A	XP_011518255.1:n.1778+47G>A
XR_242782.2:n.3862+47G>A
XR_930851.1:n.3828+81G>A
NM_001348749.1:c.3608+47G>A	NP_001335678.1:n.3608+47G>A
NM_001348750.1:c.3392+47G>A	NP_001335679.1:n.3392+47G>A
NR_145966.2:n.3854+47G>A
NM_015213.4:c.3680+47G>A MANE Select	NP_056028.2:n.3680+47G>A
NM_001243254.2:c.3646+81G>A	NP_001230183.1:n.3646+81G>A
NM_001348749.2:c.3608+47G>A	NP_001335678.1:n.3608+47G>A
NM_001348750.2:c.3392+47G>A	NP_001335679.1:n.3392+47G>A