Canonical Allele Identifier: CA473040206

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163537C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141990C>A , CM000673.2:g.9141990C>A	GRCh38
NC_000011.9:g.9163537C>A , CM000673.1:g.9163537C>A	GRCh37
NC_000011.8:g.9120113C>A	NCBI36
NG_053019.1:g.128346G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3630G>T MANE Select	ENSP00000328524.3:p.Arg1210=
ENST00000525784.6:n.1492G>T
ENST00000530780.2:c.*3456G>T	ENSP00000433925.1:n.*3456G>T
ENST00000531747.2:n.3301G>T
ENST00000679446.1:n.3551G>T
ENST00000679458.1:n.5031G>T
ENST00000679460.1:n.4692G>T
ENST00000679568.1:c.3630G>T	ENSP00000505860.1:p.Arg1210=
ENST00000679745.1:n.4135G>T
ENST00000679773.1:n.2791G>T
ENST00000679926.1:n.4932G>T
ENST00000679999.1:c.*687G>T	ENSP00000505198.1:n.*687G>T
ENST00000680252.1:c.3297G>T
ENST00000680294.1:c.3423G>T	ENSP00000506113.1:p.Arg1141=
ENST00000680358.1:n.2929G>T
ENST00000680470.1:c.*1411G>T	ENSP00000505975.1:n.*1411G>T
ENST00000680554.1:c.*163G>T	ENSP00000505621.1:n.*163G>T
ENST00000680576.1:n.5106G>T
ENST00000680599.1:n.3671G>T
ENST00000680742.1:c.*163G>T	ENSP00000505206.1:n.*163G>T
ENST00000680791.1:n.2514G>T
ENST00000680885.1:n.5332G>T
ENST00000681158.1:c.3214G>T
ENST00000681203.1:c.3558G>T	ENSP00000506456.1:p.Arg1186=
ENST00000681371.1:n.3502G>T
ENST00000681425.1:n.4108G>T
ENST00000681639.1:n.1909G>T
ENST00000328194.7:c.3630G>T	ENSP00000328524.3:p.Arg1210=
ENST00000525784.5:c.566G>T
ENST00000527700.5:n.3192G>T
ENST00000528725.5:c.326G>T
ENST00000529977.5:n.1531G>T
ENST00000530044.5:c.3630G>T	ENSP00000435866.1:p.Arg1210=
ENST00000531747.1:c.866G>T
ENST00000533737.5:c.293G>T
NM_001243254.1:c.3630G>T	NP_001230183.1:p.Arg1210=
NM_015213.3:c.3630G>T	NP_056028.2:p.Arg1210=
XM_005252832.1:c.3630G>T	XP_005252889.1:p.Arg1210=
XM_011519952.1:c.3630G>T	XP_011518254.1:p.Arg1210=
XM_011519953.1:c.1728G>T	XP_011518255.1:p.Arg576=
XR_242782.2:n.3812G>T
XR_930851.1:n.3812G>T
NM_001348749.1:c.3558G>T	NP_001335678.1:p.Arg1186=
NM_001348750.1:c.3342G>T	NP_001335679.1:p.Arg1114=
NR_145966.2:n.3804G>T
NM_015213.4:c.3630G>T MANE Select	NP_056028.2:p.Arg1210=
NM_001243254.2:c.3630G>T	NP_001230183.1:p.Arg1210=
NM_001348749.2:c.3558G>T	NP_001335678.1:p.Arg1186=
NM_001348750.2:c.3342G>T	NP_001335679.1:p.Arg1114=