Canonical Allele Identifier: CA379597155

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163499C>T (hg19) ; chr11:g.9141952C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141952C>T , CM000673.2:g.9141952C>T	GRCh38
NC_000011.9:g.9163499C>T , CM000673.1:g.9163499C>T	GRCh37
NC_000011.8:g.9120075C>T	NCBI36
NG_053019.1:g.128384G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3668G>A MANE Select	ENSP00000328524.3:p.Cys1223Tyr
ENST00000525784.6:n.1530G>A
ENST00000530780.2:c.*3494G>A	ENSP00000433925.1:n.*3494G>A
ENST00000531747.2:n.3339G>A
ENST00000679446.1:n.3589G>A
ENST00000679458.1:n.5069G>A
ENST00000679460.1:n.4730G>A
ENST00000679568.1:c.3668G>A	ENSP00000505860.1:p.Cys1223Tyr
ENST00000679745.1:n.4173G>A
ENST00000679773.1:n.2829G>A
ENST00000679926.1:n.4970G>A
ENST00000679999.1:c.*725G>A	ENSP00000505198.1:n.*725G>A
ENST00000680252.1:c.3335G>A
ENST00000680294.1:c.3461G>A	ENSP00000506113.1:p.Cys1154Tyr
ENST00000680358.1:n.2967G>A
ENST00000680470.1:c.*1449G>A	ENSP00000505975.1:n.*1449G>A
ENST00000680554.1:c.*201G>A	ENSP00000505621.1:n.*201G>A
ENST00000680576.1:n.5144G>A
ENST00000680599.1:n.3709G>A
ENST00000680742.1:c.*179+22G>A	ENSP00000505206.1:n.*179+22G>A
ENST00000680791.1:n.2552G>A
ENST00000680885.1:n.5370G>A
ENST00000681158.1:c.3252G>A
ENST00000681203.1:c.3596G>A	ENSP00000506456.1:p.Cys1199Tyr
ENST00000681371.1:n.3540G>A
ENST00000681425.1:n.4146G>A
ENST00000681639.1:n.1947G>A
ENST00000328194.7:c.3668G>A	ENSP00000328524.3:p.Cys1223Tyr
ENST00000525784.5:c.604G>A
ENST00000527700.5:n.3230G>A
ENST00000528725.5:c.364G>A
ENST00000529977.5:n.1569G>A
ENST00000530044.5:c.3646+22G>A	ENSP00000435866.1:n.3646+22G>A
ENST00000531747.1:c.904G>A
ENST00000533737.5:c.331G>A
NM_001243254.1:c.3646+22G>A	NP_001230183.1:n.3646+22G>A
NM_015213.3:c.3668G>A	NP_056028.2:p.Cys1223Tyr
XM_005252832.1:c.3668G>A	XP_005252889.1:p.Cys1223Tyr
XM_011519952.1:c.3646+22G>A	XP_011518254.1:n.3646+22G>A
XM_011519953.1:c.1766G>A	XP_011518255.1:p.Cys589Tyr
XR_242782.2:n.3850G>A
XR_930851.1:n.3828+22G>A
NM_001348749.1:c.3596G>A	NP_001335678.1:p.Cys1199Tyr
NM_001348750.1:c.3380G>A	NP_001335679.1:p.Cys1127Tyr
NR_145966.2:n.3842G>A
NM_015213.4:c.3668G>A MANE Select	NP_056028.2:p.Cys1223Tyr
NM_001243254.2:c.3646+22G>A	NP_001230183.1:n.3646+22G>A
NM_001348749.2:c.3596G>A	NP_001335678.1:p.Cys1199Tyr
NM_001348750.2:c.3380G>A	NP_001335679.1:p.Cys1127Tyr