Canonical Allele Identifier: CA379597165

Gene: DENND5A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3665T>G MANE Select	ENSP00000328524.3:p.Val1222Gly
ENST00000525784.6:n.1527T>G
ENST00000530780.2:c.*3491T>G	ENSP00000433925.1:n.*3491T>G
ENST00000531747.2:n.3336T>G
ENST00000679446.1:n.3586T>G
ENST00000679458.1:n.5066T>G
ENST00000679460.1:n.4727T>G
ENST00000679568.1:c.3665T>G	ENSP00000505860.1:p.Val1222Gly
ENST00000679745.1:n.4170T>G
ENST00000679773.1:n.2826T>G
ENST00000679926.1:n.4967T>G
ENST00000679999.1:c.*722T>G	ENSP00000505198.1:n.*722T>G
ENST00000680252.1:c.3332T>G
ENST00000680294.1:c.3458T>G	ENSP00000506113.1:p.Val1153Gly
ENST00000680358.1:n.2964T>G
ENST00000680470.1:c.*1446T>G	ENSP00000505975.1:n.*1446T>G
ENST00000680554.1:c.*198T>G	ENSP00000505621.1:n.*198T>G
ENST00000680576.1:n.5141T>G
ENST00000680599.1:n.3706T>G
ENST00000680742.1:c.*179+19T>G	ENSP00000505206.1:n.*179+19T>G
ENST00000680791.1:n.2549T>G
ENST00000680885.1:n.5367T>G
ENST00000681158.1:c.3249T>G
ENST00000681203.1:c.3593T>G	ENSP00000506456.1:p.Val1198Gly
ENST00000681371.1:n.3537T>G
ENST00000681425.1:n.4143T>G
ENST00000681639.1:n.1944T>G
ENST00000328194.7:c.3665T>G	ENSP00000328524.3:p.Val1222Gly
ENST00000525784.5:c.601T>G
ENST00000527700.5:n.3227T>G
ENST00000528725.5:c.361T>G
ENST00000529977.5:n.1566T>G
ENST00000530044.5:c.3646+19T>G	ENSP00000435866.1:n.3646+19T>G
ENST00000531747.1:c.901T>G
ENST00000533737.5:c.328T>G
NM_001243254.1:c.3646+19T>G	NP_001230183.1:n.3646+19T>G
NM_015213.3:c.3665T>G	NP_056028.2:p.Val1222Gly
XM_005252832.1:c.3665T>G	XP_005252889.1:p.Val1222Gly
XM_011519952.1:c.3646+19T>G	XP_011518254.1:n.3646+19T>G
XM_011519953.1:c.1763T>G	XP_011518255.1:p.Val588Gly
XR_242782.2:n.3847T>G
XR_930851.1:n.3828+19T>G
NM_001348749.1:c.3593T>G	NP_001335678.1:p.Val1198Gly
NM_001348750.1:c.3377T>G	NP_001335679.1:p.Val1126Gly
NR_145966.2:n.3839T>G
NM_015213.4:c.3665T>G MANE Select	NP_056028.2:p.Val1222Gly
NM_001243254.2:c.3646+19T>G	NP_001230183.1:n.3646+19T>G
NM_001348749.2:c.3593T>G	NP_001335678.1:p.Val1198Gly
NM_001348750.2:c.3377T>G	NP_001335679.1:p.Val1126Gly