Canonical Allele Identifier: CA379597551

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163545T>A (hg19) ; chr11:g.9141998T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141998T>A , CM000673.2:g.9141998T>A	GRCh38
NC_000011.9:g.9163545T>A , CM000673.1:g.9163545T>A	GRCh37
NC_000011.8:g.9120121T>A	NCBI36
NG_053019.1:g.128338A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3622A>T MANE Select	ENSP00000328524.3:p.Thr1208Ser
ENST00000525784.6:n.1484A>T
ENST00000530780.2:c.*3448A>T	ENSP00000433925.1:n.*3448A>T
ENST00000531747.2:n.3293A>T
ENST00000679446.1:n.3543A>T
ENST00000679458.1:n.5023A>T
ENST00000679460.1:n.4684A>T
ENST00000679568.1:c.3622A>T	ENSP00000505860.1:p.Thr1208Ser
ENST00000679745.1:n.4127A>T
ENST00000679773.1:n.2783A>T
ENST00000679926.1:n.4924A>T
ENST00000679999.1:c.*679A>T	ENSP00000505198.1:n.*679A>T
ENST00000680252.1:c.3289A>T
ENST00000680294.1:c.3415A>T	ENSP00000506113.1:p.Thr1139Ser
ENST00000680358.1:n.2921A>T
ENST00000680470.1:c.*1403A>T	ENSP00000505975.1:n.*1403A>T
ENST00000680554.1:c.*155A>T	ENSP00000505621.1:n.*155A>T
ENST00000680576.1:n.5098A>T
ENST00000680599.1:n.3663A>T
ENST00000680742.1:c.*155A>T	ENSP00000505206.1:n.*155A>T
ENST00000680791.1:n.2506A>T
ENST00000680885.1:n.5324A>T
ENST00000681158.1:c.3206A>T
ENST00000681203.1:c.3550A>T	ENSP00000506456.1:p.Thr1184Ser
ENST00000681371.1:n.3494A>T
ENST00000681425.1:n.4100A>T
ENST00000681639.1:n.1901A>T
ENST00000328194.7:c.3622A>T	ENSP00000328524.3:p.Thr1208Ser
ENST00000525784.5:c.558A>T
ENST00000527700.5:n.3184A>T
ENST00000528725.5:c.318A>T
ENST00000529977.5:n.1523A>T
ENST00000530044.5:c.3622A>T	ENSP00000435866.1:p.Thr1208Ser
ENST00000531747.1:c.858A>T
ENST00000533737.5:c.285A>T
NM_001243254.1:c.3622A>T	NP_001230183.1:p.Thr1208Ser
NM_015213.3:c.3622A>T	NP_056028.2:p.Thr1208Ser
XM_005252832.1:c.3622A>T	XP_005252889.1:p.Thr1208Ser
XM_011519952.1:c.3622A>T	XP_011518254.1:p.Thr1208Ser
XM_011519953.1:c.1720A>T	XP_011518255.1:p.Thr574Ser
XR_242782.2:n.3804A>T
XR_930851.1:n.3804A>T
NM_001348749.1:c.3550A>T	NP_001335678.1:p.Thr1184Ser
NM_001348750.1:c.3334A>T	NP_001335679.1:p.Thr1112Ser
NR_145966.2:n.3796A>T
NM_015213.4:c.3622A>T MANE Select	NP_056028.2:p.Thr1208Ser
NM_001243254.2:c.3622A>T	NP_001230183.1:p.Thr1208Ser
NM_001348749.2:c.3550A>T	NP_001335678.1:p.Thr1184Ser
NM_001348750.2:c.3334A>T	NP_001335679.1:p.Thr1112Ser