Canonical Allele Identifier: CA379598247

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163649G>A (hg19) ; chr11:g.9142102G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142102G>A , CM000673.2:g.9142102G>A	GRCh38
NC_000011.9:g.9163649G>A , CM000673.1:g.9163649G>A	GRCh37
NC_000011.8:g.9120225G>A	NCBI36
NG_053019.1:g.128234C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3518C>T MANE Select	ENSP00000328524.3:p.Ala1173Val
ENST00000525784.6:n.1380C>T
ENST00000530780.2:c.*3344C>T	ENSP00000433925.1:n.*3344C>T
ENST00000531747.2:n.3189C>T
ENST00000679446.1:n.3439C>T
ENST00000679458.1:n.4919C>T
ENST00000679460.1:n.4580C>T
ENST00000679568.1:c.3518C>T	ENSP00000505860.1:p.Ala1173Val
ENST00000679745.1:n.4023C>T
ENST00000679773.1:n.2679C>T
ENST00000679926.1:n.4820C>T
ENST00000679999.1:c.*575C>T	ENSP00000505198.1:n.*575C>T
ENST00000680252.1:c.3185C>T
ENST00000680294.1:c.3311C>T	ENSP00000506113.1:p.Ala1104Val
ENST00000680358.1:n.2817C>T
ENST00000680470.1:c.*1299C>T	ENSP00000505975.1:n.*1299C>T
ENST00000680554.1:c.*51C>T	ENSP00000505621.1:n.*51C>T
ENST00000680576.1:n.4994C>T
ENST00000680599.1:n.3559C>T
ENST00000680742.1:c.*51C>T	ENSP00000505206.1:n.*51C>T
ENST00000680791.1:n.2402C>T
ENST00000680885.1:n.5220C>T
ENST00000681158.1:c.3102C>T
ENST00000681203.1:c.3446C>T	ENSP00000506456.1:p.Ala1149Val
ENST00000681371.1:n.3390C>T
ENST00000681425.1:n.3996C>T
ENST00000681639.1:n.1797C>T
ENST00000328194.7:c.3518C>T	ENSP00000328524.3:p.Ala1173Val
ENST00000525784.5:c.454C>T
ENST00000527700.5:n.3080C>T
ENST00000528725.5:c.214C>T
ENST00000529977.5:n.1419C>T
ENST00000530044.5:c.3518C>T	ENSP00000435866.1:p.Ala1173Val
ENST00000531747.1:c.754C>T
ENST00000533737.5:c.181C>T
NM_001243254.1:c.3518C>T	NP_001230183.1:p.Ala1173Val
NM_015213.3:c.3518C>T	NP_056028.2:p.Ala1173Val
XM_005252832.1:c.3518C>T	XP_005252889.1:p.Ala1173Val
XM_011519952.1:c.3518C>T	XP_011518254.1:p.Ala1173Val
XM_011519953.1:c.1616C>T	XP_011518255.1:p.Ala539Val
XR_242782.2:n.3700C>T
XR_930851.1:n.3700C>T
NM_001348749.1:c.3446C>T	NP_001335678.1:p.Ala1149Val
NM_001348750.1:c.3230C>T	NP_001335679.1:p.Ala1077Val
NR_145966.2:n.3692C>T
NM_015213.4:c.3518C>T MANE Select	NP_056028.2:p.Ala1173Val
NM_001243254.2:c.3518C>T	NP_001230183.1:p.Ala1173Val
NM_001348749.2:c.3446C>T	NP_001335678.1:p.Ala1149Val
NM_001348750.2:c.3230C>T	NP_001335679.1:p.Ala1077Val