Canonical Allele Identifier: CA473040240

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163582G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142035G>C , CM000673.2:g.9142035G>C	GRCh38
NC_000011.9:g.9163582G>C , CM000673.1:g.9163582G>C	GRCh37
NC_000011.8:g.9120158G>C	NCBI36
NG_053019.1:g.128301C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3585C>G MANE Select	ENSP00000328524.3:p.Ala1195=
ENST00000525784.6:n.1447C>G
ENST00000530780.2:c.*3411C>G	ENSP00000433925.1:n.*3411C>G
ENST00000531747.2:n.3256C>G
ENST00000679446.1:n.3506C>G
ENST00000679458.1:n.4986C>G
ENST00000679460.1:n.4647C>G
ENST00000679568.1:c.3585C>G	ENSP00000505860.1:p.Ala1195=
ENST00000679745.1:n.4090C>G
ENST00000679773.1:n.2746C>G
ENST00000679926.1:n.4887C>G
ENST00000679999.1:c.*642C>G	ENSP00000505198.1:n.*642C>G
ENST00000680252.1:c.3252C>G
ENST00000680294.1:c.3378C>G	ENSP00000506113.1:p.Ala1126=
ENST00000680358.1:n.2884C>G
ENST00000680470.1:c.*1366C>G	ENSP00000505975.1:n.*1366C>G
ENST00000680554.1:c.*118C>G	ENSP00000505621.1:n.*118C>G
ENST00000680576.1:n.5061C>G
ENST00000680599.1:n.3626C>G
ENST00000680742.1:c.*118C>G	ENSP00000505206.1:n.*118C>G
ENST00000680791.1:n.2469C>G
ENST00000680885.1:n.5287C>G
ENST00000681158.1:c.3169C>G
ENST00000681203.1:c.3513C>G	ENSP00000506456.1:p.Ala1171=
ENST00000681371.1:n.3457C>G
ENST00000681425.1:n.4063C>G
ENST00000681639.1:n.1864C>G
ENST00000328194.7:c.3585C>G	ENSP00000328524.3:p.Ala1195=
ENST00000525784.5:c.521C>G
ENST00000527700.5:n.3147C>G
ENST00000528725.5:c.281C>G
ENST00000529977.5:n.1486C>G
ENST00000530044.5:c.3585C>G	ENSP00000435866.1:p.Ala1195=
ENST00000531747.1:c.821C>G
ENST00000533737.5:c.248C>G
NM_001243254.1:c.3585C>G	NP_001230183.1:p.Ala1195=
NM_015213.3:c.3585C>G	NP_056028.2:p.Ala1195=
XM_005252832.1:c.3585C>G	XP_005252889.1:p.Ala1195=
XM_011519952.1:c.3585C>G	XP_011518254.1:p.Ala1195=
XM_011519953.1:c.1683C>G	XP_011518255.1:p.Ala561=
XR_242782.2:n.3767C>G
XR_930851.1:n.3767C>G
NM_001348749.1:c.3513C>G	NP_001335678.1:p.Ala1171=
NM_001348750.1:c.3297C>G	NP_001335679.1:p.Ala1099=
NR_145966.2:n.3759C>G
NM_015213.4:c.3585C>G MANE Select	NP_056028.2:p.Ala1195=
NM_001243254.2:c.3585C>G	NP_001230183.1:p.Ala1195=
NM_001348749.2:c.3513C>G	NP_001335678.1:p.Ala1171=
NM_001348750.2:c.3297C>G	NP_001335679.1:p.Ala1099=