Canonical Allele Identifier: CA379597861

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163593G>C (hg19) ; chr11:g.9142046G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142046G>C , CM000673.2:g.9142046G>C	GRCh38
NC_000011.9:g.9163593G>C , CM000673.1:g.9163593G>C	GRCh37
NC_000011.8:g.9120169G>C	NCBI36
NG_053019.1:g.128290C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3574C>G MANE Select	ENSP00000328524.3:p.His1192Asp
ENST00000525784.6:n.1436C>G
ENST00000530780.2:c.*3400C>G	ENSP00000433925.1:n.*3400C>G
ENST00000531747.2:n.3245C>G
ENST00000679446.1:n.3495C>G
ENST00000679458.1:n.4975C>G
ENST00000679460.1:n.4636C>G
ENST00000679568.1:c.3574C>G	ENSP00000505860.1:p.His1192Asp
ENST00000679745.1:n.4079C>G
ENST00000679773.1:n.2735C>G
ENST00000679926.1:n.4876C>G
ENST00000679999.1:c.*631C>G	ENSP00000505198.1:n.*631C>G
ENST00000680252.1:c.3241C>G
ENST00000680294.1:c.3367C>G	ENSP00000506113.1:p.His1123Asp
ENST00000680358.1:n.2873C>G
ENST00000680470.1:c.*1355C>G	ENSP00000505975.1:n.*1355C>G
ENST00000680554.1:c.*107C>G	ENSP00000505621.1:n.*107C>G
ENST00000680576.1:n.5050C>G
ENST00000680599.1:n.3615C>G
ENST00000680742.1:c.*107C>G	ENSP00000505206.1:n.*107C>G
ENST00000680791.1:n.2458C>G
ENST00000680885.1:n.5276C>G
ENST00000681158.1:c.3158C>G
ENST00000681203.1:c.3502C>G	ENSP00000506456.1:p.His1168Asp
ENST00000681371.1:n.3446C>G
ENST00000681425.1:n.4052C>G
ENST00000681639.1:n.1853C>G
ENST00000328194.7:c.3574C>G	ENSP00000328524.3:p.His1192Asp
ENST00000525784.5:c.510C>G
ENST00000527700.5:n.3136C>G
ENST00000528725.5:c.270C>G
ENST00000529977.5:n.1475C>G
ENST00000530044.5:c.3574C>G	ENSP00000435866.1:p.His1192Asp
ENST00000531747.1:c.810C>G
ENST00000533737.5:c.237C>G
NM_001243254.1:c.3574C>G	NP_001230183.1:p.His1192Asp
NM_015213.3:c.3574C>G	NP_056028.2:p.His1192Asp
XM_005252832.1:c.3574C>G	XP_005252889.1:p.His1192Asp
XM_011519952.1:c.3574C>G	XP_011518254.1:p.His1192Asp
XM_011519953.1:c.1672C>G	XP_011518255.1:p.His558Asp
XR_242782.2:n.3756C>G
XR_930851.1:n.3756C>G
NM_001348749.1:c.3502C>G	NP_001335678.1:p.His1168Asp
NM_001348750.1:c.3286C>G	NP_001335679.1:p.His1096Asp
NR_145966.2:n.3748C>G
NM_015213.4:c.3574C>G MANE Select	NP_056028.2:p.His1192Asp
NM_001243254.2:c.3574C>G	NP_001230183.1:p.His1192Asp
NM_001348749.2:c.3502C>G	NP_001335678.1:p.His1168Asp
NM_001348750.2:c.3286C>G	NP_001335679.1:p.His1096Asp