Canonical Allele Identifier: CA379597926

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163598T>A (hg19) ; chr11:g.9142051T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142051T>A , CM000673.2:g.9142051T>A	GRCh38
NC_000011.9:g.9163598T>A , CM000673.1:g.9163598T>A	GRCh37
NC_000011.8:g.9120174T>A	NCBI36
NG_053019.1:g.128285A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3569A>T MANE Select	ENSP00000328524.3:p.Asn1190Ile
ENST00000525784.6:n.1431A>T
ENST00000530780.2:c.*3395A>T	ENSP00000433925.1:n.*3395A>T
ENST00000531747.2:n.3240A>T
ENST00000679446.1:n.3490A>T
ENST00000679458.1:n.4970A>T
ENST00000679460.1:n.4631A>T
ENST00000679568.1:c.3569A>T	ENSP00000505860.1:p.Asn1190Ile
ENST00000679745.1:n.4074A>T
ENST00000679773.1:n.2730A>T
ENST00000679926.1:n.4871A>T
ENST00000679999.1:c.*626A>T	ENSP00000505198.1:n.*626A>T
ENST00000680252.1:c.3236A>T
ENST00000680294.1:c.3362A>T	ENSP00000506113.1:p.Asn1121Ile
ENST00000680358.1:n.2868A>T
ENST00000680470.1:c.*1350A>T	ENSP00000505975.1:n.*1350A>T
ENST00000680554.1:c.*102A>T	ENSP00000505621.1:n.*102A>T
ENST00000680576.1:n.5045A>T
ENST00000680599.1:n.3610A>T
ENST00000680742.1:c.*102A>T	ENSP00000505206.1:n.*102A>T
ENST00000680791.1:n.2453A>T
ENST00000680885.1:n.5271A>T
ENST00000681158.1:c.3153A>T
ENST00000681203.1:c.3497A>T	ENSP00000506456.1:p.Asn1166Ile
ENST00000681371.1:n.3441A>T
ENST00000681425.1:n.4047A>T
ENST00000681639.1:n.1848A>T
ENST00000328194.7:c.3569A>T	ENSP00000328524.3:p.Asn1190Ile
ENST00000525784.5:c.505A>T
ENST00000527700.5:n.3131A>T
ENST00000528725.5:c.265A>T
ENST00000529977.5:n.1470A>T
ENST00000530044.5:c.3569A>T	ENSP00000435866.1:p.Asn1190Ile
ENST00000531747.1:c.805A>T
ENST00000533737.5:c.232A>T
NM_001243254.1:c.3569A>T	NP_001230183.1:p.Asn1190Ile
NM_015213.3:c.3569A>T	NP_056028.2:p.Asn1190Ile
XM_005252832.1:c.3569A>T	XP_005252889.1:p.Asn1190Ile
XM_011519952.1:c.3569A>T	XP_011518254.1:p.Asn1190Ile
XM_011519953.1:c.1667A>T	XP_011518255.1:p.Asn556Ile
XR_242782.2:n.3751A>T
XR_930851.1:n.3751A>T
NM_001348749.1:c.3497A>T	NP_001335678.1:p.Asn1166Ile
NM_001348750.1:c.3281A>T	NP_001335679.1:p.Asn1094Ile
NR_145966.2:n.3743A>T
NM_015213.4:c.3569A>T MANE Select	NP_056028.2:p.Asn1190Ile
NM_001243254.2:c.3569A>T	NP_001230183.1:p.Asn1190Ile
NM_001348749.2:c.3497A>T	NP_001335678.1:p.Asn1166Ile
NM_001348750.2:c.3281A>T	NP_001335679.1:p.Asn1094Ile