Canonical Allele Identifier: CA379597702

Gene: DENND5A

Linked Data

• dbSNP Id: rs1554909103
• MyVariant Identifiers: chr11:g.9163570G>T (hg19) ; chr11:g.9142023G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142023G>T , CM000673.2:g.9142023G>T	GRCh38
NC_000011.9:g.9163570G>T , CM000673.1:g.9163570G>T	GRCh37
NC_000011.8:g.9120146G>T	NCBI36
NG_053019.1:g.128313C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3597C>A MANE Select	ENSP00000328524.3:p.Cys1199Ter
ENST00000525784.6:n.1459C>A
ENST00000530780.2:c.*3423C>A	ENSP00000433925.1:n.*3423C>A
ENST00000531747.2:n.3268C>A
ENST00000679446.1:n.3518C>A
ENST00000679458.1:n.4998C>A
ENST00000679460.1:n.4659C>A
ENST00000679568.1:c.3597C>A	ENSP00000505860.1:p.Cys1199Ter
ENST00000679745.1:n.4102C>A
ENST00000679773.1:n.2758C>A
ENST00000679926.1:n.4899C>A
ENST00000679999.1:c.*654C>A	ENSP00000505198.1:n.*654C>A
ENST00000680252.1:c.3264C>A
ENST00000680294.1:c.3390C>A	ENSP00000506113.1:p.Cys1130Ter
ENST00000680358.1:n.2896C>A
ENST00000680470.1:c.*1378C>A	ENSP00000505975.1:n.*1378C>A
ENST00000680554.1:c.*130C>A	ENSP00000505621.1:n.*130C>A
ENST00000680576.1:n.5073C>A
ENST00000680599.1:n.3638C>A
ENST00000680742.1:c.*130C>A	ENSP00000505206.1:n.*130C>A
ENST00000680791.1:n.2481C>A
ENST00000680885.1:n.5299C>A
ENST00000681158.1:c.3181C>A
ENST00000681203.1:c.3525C>A	ENSP00000506456.1:p.Cys1175Ter
ENST00000681371.1:n.3469C>A
ENST00000681425.1:n.4075C>A
ENST00000681639.1:n.1876C>A
ENST00000328194.7:c.3597C>A	ENSP00000328524.3:p.Cys1199Ter
ENST00000525784.5:c.533C>A
ENST00000527700.5:n.3159C>A
ENST00000528725.5:c.293C>A
ENST00000529977.5:n.1498C>A
ENST00000530044.5:c.3597C>A	ENSP00000435866.1:p.Cys1199Ter
ENST00000531747.1:c.833C>A
ENST00000533737.5:c.260C>A
NM_001243254.1:c.3597C>A	NP_001230183.1:p.Cys1199Ter
NM_015213.3:c.3597C>A	NP_056028.2:p.Cys1199Ter
XM_005252832.1:c.3597C>A	XP_005252889.1:p.Cys1199Ter
XM_011519952.1:c.3597C>A	XP_011518254.1:p.Cys1199Ter
XM_011519953.1:c.1695C>A	XP_011518255.1:p.Cys565Ter
XR_242782.2:n.3779C>A
XR_930851.1:n.3779C>A
NM_001348749.1:c.3525C>A	NP_001335678.1:p.Cys1175Ter
NM_001348750.1:c.3309C>A	NP_001335679.1:p.Cys1103Ter
NR_145966.2:n.3771C>A
NM_015213.4:c.3597C>A MANE Select	NP_056028.2:p.Cys1199Ter
NM_001243254.2:c.3597C>A	NP_001230183.1:p.Cys1199Ter
NM_001348749.2:c.3525C>A	NP_001335678.1:p.Cys1175Ter
NM_001348750.2:c.3309C>A	NP_001335679.1:p.Cys1103Ter