Canonical Allele Identifier: CA379597877

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163594C>G (hg19) ; chr11:g.9142047C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142047C>G , CM000673.2:g.9142047C>G	GRCh38
NC_000011.9:g.9163594C>G , CM000673.1:g.9163594C>G	GRCh37
NC_000011.8:g.9120170C>G	NCBI36
NG_053019.1:g.128289G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3573G>C MANE Select	ENSP00000328524.3:p.Trp1191Cys
ENST00000525784.6:n.1435G>C
ENST00000530780.2:c.*3399G>C	ENSP00000433925.1:n.*3399G>C
ENST00000531747.2:n.3244G>C
ENST00000679446.1:n.3494G>C
ENST00000679458.1:n.4974G>C
ENST00000679460.1:n.4635G>C
ENST00000679568.1:c.3573G>C	ENSP00000505860.1:p.Trp1191Cys
ENST00000679745.1:n.4078G>C
ENST00000679773.1:n.2734G>C
ENST00000679926.1:n.4875G>C
ENST00000679999.1:c.*630G>C	ENSP00000505198.1:n.*630G>C
ENST00000680252.1:c.3240G>C
ENST00000680294.1:c.3366G>C	ENSP00000506113.1:p.Trp1122Cys
ENST00000680358.1:n.2872G>C
ENST00000680470.1:c.*1354G>C	ENSP00000505975.1:n.*1354G>C
ENST00000680554.1:c.*106G>C	ENSP00000505621.1:n.*106G>C
ENST00000680576.1:n.5049G>C
ENST00000680599.1:n.3614G>C
ENST00000680742.1:c.*106G>C	ENSP00000505206.1:n.*106G>C
ENST00000680791.1:n.2457G>C
ENST00000680885.1:n.5275G>C
ENST00000681158.1:c.3157G>C
ENST00000681203.1:c.3501G>C	ENSP00000506456.1:p.Trp1167Cys
ENST00000681371.1:n.3445G>C
ENST00000681425.1:n.4051G>C
ENST00000681639.1:n.1852G>C
ENST00000328194.7:c.3573G>C	ENSP00000328524.3:p.Trp1191Cys
ENST00000525784.5:c.509G>C
ENST00000527700.5:n.3135G>C
ENST00000528725.5:c.269G>C
ENST00000529977.5:n.1474G>C
ENST00000530044.5:c.3573G>C	ENSP00000435866.1:p.Trp1191Cys
ENST00000531747.1:c.809G>C
ENST00000533737.5:c.236G>C
NM_001243254.1:c.3573G>C	NP_001230183.1:p.Trp1191Cys
NM_015213.3:c.3573G>C	NP_056028.2:p.Trp1191Cys
XM_005252832.1:c.3573G>C	XP_005252889.1:p.Trp1191Cys
XM_011519952.1:c.3573G>C	XP_011518254.1:p.Trp1191Cys
XM_011519953.1:c.1671G>C	XP_011518255.1:p.Trp557Cys
XR_242782.2:n.3755G>C
XR_930851.1:n.3755G>C
NM_001348749.1:c.3501G>C	NP_001335678.1:p.Trp1167Cys
NM_001348750.1:c.3285G>C	NP_001335679.1:p.Trp1095Cys
NR_145966.2:n.3747G>C
NM_015213.4:c.3573G>C MANE Select	NP_056028.2:p.Trp1191Cys
NM_001243254.2:c.3573G>C	NP_001230183.1:p.Trp1191Cys
NM_001348749.2:c.3501G>C	NP_001335678.1:p.Trp1167Cys
NM_001348750.2:c.3285G>C	NP_001335679.1:p.Trp1095Cys