Canonical Allele Identifier: CA379597237

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163511T>G (hg19) ; chr11:g.9141964T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141964T>G , CM000673.2:g.9141964T>G	GRCh38
NC_000011.9:g.9163511T>G , CM000673.1:g.9163511T>G	GRCh37
NC_000011.8:g.9120087T>G	NCBI36
NG_053019.1:g.128372A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3656A>C MANE Select	ENSP00000328524.3:p.Gln1219Pro
ENST00000525784.6:n.1518A>C
ENST00000530780.2:c.*3482A>C	ENSP00000433925.1:n.*3482A>C
ENST00000531747.2:n.3327A>C
ENST00000679446.1:n.3577A>C
ENST00000679458.1:n.5057A>C
ENST00000679460.1:n.4718A>C
ENST00000679568.1:c.3656A>C	ENSP00000505860.1:p.Gln1219Pro
ENST00000679745.1:n.4161A>C
ENST00000679773.1:n.2817A>C
ENST00000679926.1:n.4958A>C
ENST00000679999.1:c.*713A>C	ENSP00000505198.1:n.*713A>C
ENST00000680252.1:c.3323A>C
ENST00000680294.1:c.3449A>C	ENSP00000506113.1:p.Gln1150Pro
ENST00000680358.1:n.2955A>C
ENST00000680470.1:c.*1437A>C	ENSP00000505975.1:n.*1437A>C
ENST00000680554.1:c.*189A>C	ENSP00000505621.1:n.*189A>C
ENST00000680576.1:n.5132A>C
ENST00000680599.1:n.3697A>C
ENST00000680742.1:c.*179+10A>C	ENSP00000505206.1:n.*179+10A>C
ENST00000680791.1:n.2540A>C
ENST00000680885.1:n.5358A>C
ENST00000681158.1:c.3240A>C
ENST00000681203.1:c.3584A>C	ENSP00000506456.1:p.Gln1195Pro
ENST00000681371.1:n.3528A>C
ENST00000681425.1:n.4134A>C
ENST00000681639.1:n.1935A>C
ENST00000328194.7:c.3656A>C	ENSP00000328524.3:p.Gln1219Pro
ENST00000525784.5:c.592A>C
ENST00000527700.5:n.3218A>C
ENST00000528725.5:c.352A>C
ENST00000529977.5:n.1557A>C
ENST00000530044.5:c.3646+10A>C	ENSP00000435866.1:n.3646+10A>C
ENST00000531747.1:c.892A>C
ENST00000533737.5:c.319A>C
NM_001243254.1:c.3646+10A>C	NP_001230183.1:n.3646+10A>C
NM_015213.3:c.3656A>C	NP_056028.2:p.Gln1219Pro
XM_005252832.1:c.3656A>C	XP_005252889.1:p.Gln1219Pro
XM_011519952.1:c.3646+10A>C	XP_011518254.1:n.3646+10A>C
XM_011519953.1:c.1754A>C	XP_011518255.1:p.Gln585Pro
XR_242782.2:n.3838A>C
XR_930851.1:n.3828+10A>C
NM_001348749.1:c.3584A>C	NP_001335678.1:p.Gln1195Pro
NM_001348750.1:c.3368A>C	NP_001335679.1:p.Gln1123Pro
NR_145966.2:n.3830A>C
NM_015213.4:c.3656A>C MANE Select	NP_056028.2:p.Gln1219Pro
NM_001243254.2:c.3646+10A>C	NP_001230183.1:n.3646+10A>C
NM_001348749.2:c.3584A>C	NP_001335678.1:p.Gln1195Pro
NM_001348750.2:c.3368A>C	NP_001335679.1:p.Gln1123Pro