Canonical Allele Identifier: CA5876943

Gene: DENND5A

Linked Data

• dbSNP Id: rs745622715
• ExAC: 11:9161172 G / A
• gnomAD v2: 11-9161172-G-A
• gnomAD v3: 11-9139625-G-A
• gnomAD v4: 11-9139625-G-A
• MyVariant Identifiers: chr11:g.9161172G>A (hg19) ; chr11:g.9139625G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9139625G>A , CM000673.2:g.9139625G>A	GRCh38
NC_000011.9:g.9161172G>A , CM000673.1:g.9161172G>A	GRCh37
NC_000011.8:g.9117748G>A	NCBI36
NG_053019.1:g.130711C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.*46C>T MANE Select	ENSP00000328524.3:n.*46C>T
ENST00000525784.6:n.1772C>T
ENST00000530780.2:c.*3736C>T	ENSP00000433925.1:n.*3736C>T
ENST00000531747.2:n.3581C>T
ENST00000679446.1:n.5916C>T
ENST00000679458.1:n.5311C>T
ENST00000679460.1:n.4972C>T
ENST00000679568.1:c.*46C>T	ENSP00000505860.1:n.*46C>T
ENST00000679745.1:n.4415C>T
ENST00000679773.1:n.3071C>T
ENST00000679926.1:n.5212C>T
ENST00000679999.1:c.*967C>T	ENSP00000505198.1:n.*967C>T
ENST00000680252.1:c.3577C>T
ENST00000680294.1:c.*46C>T	ENSP00000506113.1:n.*46C>T
ENST00000680358.1:n.3209C>T
ENST00000680470.1:c.*1691C>T	ENSP00000505975.1:n.*1691C>T
ENST00000680554.1:c.*443C>T	ENSP00000505621.1:n.*443C>T
ENST00000680576.1:n.7471C>T
ENST00000680599.1:n.3951C>T
ENST00000680742.1:c.*409C>T	ENSP00000505206.1:n.*409C>T
ENST00000680791.1:n.2794C>T
ENST00000680885.1:n.5612C>T
ENST00000681158.1:c.3494C>T
ENST00000681203.1:c.*46C>T	ENSP00000506456.1:n.*46C>T
ENST00000681371.1:n.3782C>T
ENST00000681425.1:n.4388C>T
ENST00000681639.1:n.2189C>T
ENST00000328194.7:c.*46C>T	ENSP00000328524.3:n.*46C>T
ENST00000527700.5:n.3472C>T
ENST00000528725.5:c.606C>T
ENST00000529977.5:n.1811C>T
ENST00000530044.5:c.*150C>T	ENSP00000435866.1:n.*150C>T
ENST00000533737.5:c.633C>T
NM_001243254.1:c.*150C>T	NP_001230183.1:n.*150C>T
NM_015213.3:c.*46C>T	NP_056028.2:n.*46C>T
XM_005252832.1:c.*46C>T	XP_005252889.1:n.*46C>T
XM_011519953.1:c.*46C>T	XP_011518255.1:n.*46C>T
XR_242782.2:n.4092C>T
XR_930851.1:n.4058C>T
NM_001348749.1:c.*46C>T	NP_001335678.1:n.*46C>T
NM_001348750.1:c.*46C>T	NP_001335679.1:n.*46C>T
NR_145966.2:n.4084C>T
NM_015213.4:c.*46C>T MANE Select	NP_056028.2:n.*46C>T
NM_001243254.2:c.*150C>T	NP_001230183.1:n.*150C>T
NM_001348749.2:c.*46C>T	NP_001335678.1:n.*46C>T
NM_001348750.2:c.*46C>T	NP_001335679.1:n.*46C>T