Canonical Allele Identifier: CA379597166

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163502A>T (hg19) ; chr11:g.9141955A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141955A>T , CM000673.2:g.9141955A>T	GRCh38
NC_000011.9:g.9163502A>T , CM000673.1:g.9163502A>T	GRCh37
NC_000011.8:g.9120078A>T	NCBI36
NG_053019.1:g.128381T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3665T>A MANE Select	ENSP00000328524.3:p.Val1222Glu
ENST00000525784.6:n.1527T>A
ENST00000530780.2:c.*3491T>A	ENSP00000433925.1:n.*3491T>A
ENST00000531747.2:n.3336T>A
ENST00000679446.1:n.3586T>A
ENST00000679458.1:n.5066T>A
ENST00000679460.1:n.4727T>A
ENST00000679568.1:c.3665T>A	ENSP00000505860.1:p.Val1222Glu
ENST00000679745.1:n.4170T>A
ENST00000679773.1:n.2826T>A
ENST00000679926.1:n.4967T>A
ENST00000679999.1:c.*722T>A	ENSP00000505198.1:n.*722T>A
ENST00000680252.1:c.3332T>A
ENST00000680294.1:c.3458T>A	ENSP00000506113.1:p.Val1153Glu
ENST00000680358.1:n.2964T>A
ENST00000680470.1:c.*1446T>A	ENSP00000505975.1:n.*1446T>A
ENST00000680554.1:c.*198T>A	ENSP00000505621.1:n.*198T>A
ENST00000680576.1:n.5141T>A
ENST00000680599.1:n.3706T>A
ENST00000680742.1:c.*179+19T>A	ENSP00000505206.1:n.*179+19T>A
ENST00000680791.1:n.2549T>A
ENST00000680885.1:n.5367T>A
ENST00000681158.1:c.3249T>A
ENST00000681203.1:c.3593T>A	ENSP00000506456.1:p.Val1198Glu
ENST00000681371.1:n.3537T>A
ENST00000681425.1:n.4143T>A
ENST00000681639.1:n.1944T>A
ENST00000328194.7:c.3665T>A	ENSP00000328524.3:p.Val1222Glu
ENST00000525784.5:c.601T>A
ENST00000527700.5:n.3227T>A
ENST00000528725.5:c.361T>A
ENST00000529977.5:n.1566T>A
ENST00000530044.5:c.3646+19T>A	ENSP00000435866.1:n.3646+19T>A
ENST00000531747.1:c.901T>A
ENST00000533737.5:c.328T>A
NM_001243254.1:c.3646+19T>A	NP_001230183.1:n.3646+19T>A
NM_015213.3:c.3665T>A	NP_056028.2:p.Val1222Glu
XM_005252832.1:c.3665T>A	XP_005252889.1:p.Val1222Glu
XM_011519952.1:c.3646+19T>A	XP_011518254.1:n.3646+19T>A
XM_011519953.1:c.1763T>A	XP_011518255.1:p.Val588Glu
XR_242782.2:n.3847T>A
XR_930851.1:n.3828+19T>A
NM_001348749.1:c.3593T>A	NP_001335678.1:p.Val1198Glu
NM_001348750.1:c.3377T>A	NP_001335679.1:p.Val1126Glu
NR_145966.2:n.3839T>A
NM_015213.4:c.3665T>A MANE Select	NP_056028.2:p.Val1222Glu
NM_001243254.2:c.3646+19T>A	NP_001230183.1:n.3646+19T>A
NM_001348749.2:c.3593T>A	NP_001335678.1:p.Val1198Glu
NM_001348750.2:c.3377T>A	NP_001335679.1:p.Val1126Glu