Canonical Allele Identifier: CA379597480

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163536T>A (hg19) ; chr11:g.9141989T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141989T>A , CM000673.2:g.9141989T>A	GRCh38
NC_000011.9:g.9163536T>A , CM000673.1:g.9163536T>A	GRCh37
NC_000011.8:g.9120112T>A	NCBI36
NG_053019.1:g.128347A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3631A>T MANE Select	ENSP00000328524.3:p.Asn1211Tyr
ENST00000525784.6:n.1493A>T
ENST00000530780.2:c.*3457A>T	ENSP00000433925.1:n.*3457A>T
ENST00000531747.2:n.3302A>T
ENST00000679446.1:n.3552A>T
ENST00000679458.1:n.5032A>T
ENST00000679460.1:n.4693A>T
ENST00000679568.1:c.3631A>T	ENSP00000505860.1:p.Asn1211Tyr
ENST00000679745.1:n.4136A>T
ENST00000679773.1:n.2792A>T
ENST00000679926.1:n.4933A>T
ENST00000679999.1:c.*688A>T	ENSP00000505198.1:n.*688A>T
ENST00000680252.1:c.3298A>T
ENST00000680294.1:c.3424A>T	ENSP00000506113.1:p.Asn1142Tyr
ENST00000680358.1:n.2930A>T
ENST00000680470.1:c.*1412A>T	ENSP00000505975.1:n.*1412A>T
ENST00000680554.1:c.*164A>T	ENSP00000505621.1:n.*164A>T
ENST00000680576.1:n.5107A>T
ENST00000680599.1:n.3672A>T
ENST00000680742.1:c.*164A>T	ENSP00000505206.1:n.*164A>T
ENST00000680791.1:n.2515A>T
ENST00000680885.1:n.5333A>T
ENST00000681158.1:c.3215A>T
ENST00000681203.1:c.3559A>T	ENSP00000506456.1:p.Asn1187Tyr
ENST00000681371.1:n.3503A>T
ENST00000681425.1:n.4109A>T
ENST00000681639.1:n.1910A>T
ENST00000328194.7:c.3631A>T	ENSP00000328524.3:p.Asn1211Tyr
ENST00000525784.5:c.567A>T
ENST00000527700.5:n.3193A>T
ENST00000528725.5:c.327A>T
ENST00000529977.5:n.1532A>T
ENST00000530044.5:c.3631A>T	ENSP00000435866.1:p.Asn1211Tyr
ENST00000531747.1:c.867A>T
ENST00000533737.5:c.294A>T
NM_001243254.1:c.3631A>T	NP_001230183.1:p.Asn1211Tyr
NM_015213.3:c.3631A>T	NP_056028.2:p.Asn1211Tyr
XM_005252832.1:c.3631A>T	XP_005252889.1:p.Asn1211Tyr
XM_011519952.1:c.3631A>T	XP_011518254.1:p.Asn1211Tyr
XM_011519953.1:c.1729A>T	XP_011518255.1:p.Asn577Tyr
XR_242782.2:n.3813A>T
XR_930851.1:n.3813A>T
NM_001348749.1:c.3559A>T	NP_001335678.1:p.Asn1187Tyr
NM_001348750.1:c.3343A>T	NP_001335679.1:p.Asn1115Tyr
NR_145966.2:n.3805A>T
NM_015213.4:c.3631A>T MANE Select	NP_056028.2:p.Asn1211Tyr
NM_001243254.2:c.3631A>T	NP_001230183.1:p.Asn1211Tyr
NM_001348749.2:c.3559A>T	NP_001335678.1:p.Asn1187Tyr
NM_001348750.2:c.3343A>T	NP_001335679.1:p.Asn1115Tyr