Canonical Allele Identifier: CA5877275

Gene: DENND5A

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9150228A>G , CM000673.2:g.9150228A>G	GRCh38
NC_000011.9:g.9171775A>G , CM000673.1:g.9171775A>G	GRCh37
NC_000011.8:g.9128351A>G	NCBI36
NG_053019.1:g.120108T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2607-19T>C MANE Select	ENSP00000328524.3:n.2607-19T>C
ENST00000530780.2:c.*2433-19T>C	ENSP00000433925.1:n.*2433-19T>C
ENST00000679446.1:n.2528-19T>C
ENST00000679458.1:n.4008-19T>C
ENST00000679460.1:n.2396-19T>C
ENST00000679568.1:c.2607-19T>C	ENSP00000505860.1:n.2607-19T>C
ENST00000679745.1:n.2396-19T>C
ENST00000679926.1:n.1423-19T>C
ENST00000679999.1:c.2607-19T>C	ENSP00000505198.1:n.2607-19T>C
ENST00000680252.1:c.2396-19T>C
ENST00000680294.1:c.2607-19T>C	ENSP00000506113.1:n.2607-19T>C
ENST00000680358.1:n.1906-19T>C
ENST00000680470.1:c.*388-19T>C	ENSP00000505975.1:n.*388-19T>C
ENST00000680554.1:c.2319-19T>C	ENSP00000505621.1:n.2319-19T>C
ENST00000680576.1:n.2396-19T>C
ENST00000680599.1:n.2648-19T>C
ENST00000680742.1:c.2607-19T>C	ENSP00000505206.1:n.2607-19T>C
ENST00000680885.1:n.2528-19T>C
ENST00000681158.1:c.2396-19T>C
ENST00000681203.1:c.2535-19T>C	ENSP00000506456.1:n.2535-19T>C
ENST00000681425.1:n.2528-19T>C
ENST00000328194.7:c.2607-19T>C	ENSP00000328524.3:n.2607-19T>C
ENST00000524446.2:c.118-19T>C
ENST00000526707.5:c.*26-19T>C	ENSP00000436780.1:n.*26-19T>C
ENST00000527700.5:n.2169-19T>C
ENST00000530044.5:c.2607-19T>C	ENSP00000435866.1:n.2607-19T>C
ENST00000531580.1:n.81-19T>C
NM_001243254.1:c.2607-19T>C	NP_001230183.1:n.2607-19T>C
NM_015213.3:c.2607-19T>C	NP_056028.2:n.2607-19T>C
XM_005252832.1:c.2607-19T>C	XP_005252889.1:n.2607-19T>C
XM_011519952.1:c.2607-19T>C	XP_011518254.1:n.2607-19T>C
XM_011519953.1:c.705-19T>C	XP_011518255.1:n.705-19T>C
XR_242782.2:n.2872-19T>C
XR_930851.1:n.2872-19T>C
XR_930852.1:n.2872-19T>C
XR_930853.1:n.2721-19T>C
NM_001348749.1:c.2535-19T>C	NP_001335678.1:n.2535-19T>C
NM_001348750.1:c.2319-19T>C	NP_001335679.1:n.2319-19T>C
NR_145966.2:n.2864-19T>C
NM_015213.4:c.2607-19T>C MANE Select	NP_056028.2:n.2607-19T>C
NM_001243254.2:c.2607-19T>C	NP_001230183.1:n.2607-19T>C
NM_001348749.2:c.2535-19T>C	NP_001335678.1:n.2535-19T>C
NM_001348750.2:c.2319-19T>C	NP_001335679.1:n.2319-19T>C