Canonical Allele Identifier: CA473040252

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163606A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142059A>T , CM000673.2:g.9142059A>T	GRCh38
NC_000011.9:g.9163606A>T , CM000673.1:g.9163606A>T	GRCh37
NC_000011.8:g.9120182A>T	NCBI36
NG_053019.1:g.128277T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3561T>A MANE Select	ENSP00000328524.3:p.Pro1187=
ENST00000525784.6:n.1423T>A
ENST00000530780.2:c.*3387T>A	ENSP00000433925.1:n.*3387T>A
ENST00000531747.2:n.3232T>A
ENST00000679446.1:n.3482T>A
ENST00000679458.1:n.4962T>A
ENST00000679460.1:n.4623T>A
ENST00000679568.1:c.3561T>A	ENSP00000505860.1:p.Pro1187=
ENST00000679745.1:n.4066T>A
ENST00000679773.1:n.2722T>A
ENST00000679926.1:n.4863T>A
ENST00000679999.1:c.*618T>A	ENSP00000505198.1:n.*618T>A
ENST00000680252.1:c.3228T>A
ENST00000680294.1:c.3354T>A	ENSP00000506113.1:p.Pro1118=
ENST00000680358.1:n.2860T>A
ENST00000680470.1:c.*1342T>A	ENSP00000505975.1:n.*1342T>A
ENST00000680554.1:c.*94T>A	ENSP00000505621.1:n.*94T>A
ENST00000680576.1:n.5037T>A
ENST00000680599.1:n.3602T>A
ENST00000680742.1:c.*94T>A	ENSP00000505206.1:n.*94T>A
ENST00000680791.1:n.2445T>A
ENST00000680885.1:n.5263T>A
ENST00000681158.1:c.3145T>A
ENST00000681203.1:c.3489T>A	ENSP00000506456.1:p.Pro1163=
ENST00000681371.1:n.3433T>A
ENST00000681425.1:n.4039T>A
ENST00000681639.1:n.1840T>A
ENST00000328194.7:c.3561T>A	ENSP00000328524.3:p.Pro1187=
ENST00000525784.5:c.497T>A
ENST00000527700.5:n.3123T>A
ENST00000528725.5:c.257T>A
ENST00000529977.5:n.1462T>A
ENST00000530044.5:c.3561T>A	ENSP00000435866.1:p.Pro1187=
ENST00000531747.1:c.797T>A
ENST00000533737.5:c.224T>A
NM_001243254.1:c.3561T>A	NP_001230183.1:p.Pro1187=
NM_015213.3:c.3561T>A	NP_056028.2:p.Pro1187=
XM_005252832.1:c.3561T>A	XP_005252889.1:p.Pro1187=
XM_011519952.1:c.3561T>A	XP_011518254.1:p.Pro1187=
XM_011519953.1:c.1659T>A	XP_011518255.1:p.Pro553=
XR_242782.2:n.3743T>A
XR_930851.1:n.3743T>A
NM_001348749.1:c.3489T>A	NP_001335678.1:p.Pro1163=
NM_001348750.1:c.3273T>A	NP_001335679.1:p.Pro1091=
NR_145966.2:n.3735T>A
NM_015213.4:c.3561T>A MANE Select	NP_056028.2:p.Pro1187=
NM_001243254.2:c.3561T>A	NP_001230183.1:p.Pro1187=
NM_001348749.2:c.3489T>A	NP_001335678.1:p.Pro1163=
NM_001348750.2:c.3273T>A	NP_001335679.1:p.Pro1091=