Canonical Allele Identifier: CA473040217

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9142005-G-A
• MyVariant Identifiers: chr11:g.9163552G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142005G>A , CM000673.2:g.9142005G>A	GRCh38
NC_000011.9:g.9163552G>A , CM000673.1:g.9163552G>A	GRCh37
NC_000011.8:g.9120128G>A	NCBI36
NG_053019.1:g.128331C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3615C>T MANE Select	ENSP00000328524.3:p.Ile1205=
ENST00000525784.6:n.1477C>T
ENST00000530780.2:c.*3441C>T	ENSP00000433925.1:n.*3441C>T
ENST00000531747.2:n.3286C>T
ENST00000679446.1:n.3536C>T
ENST00000679458.1:n.5016C>T
ENST00000679460.1:n.4677C>T
ENST00000679568.1:c.3615C>T	ENSP00000505860.1:p.Ile1205=
ENST00000679745.1:n.4120C>T
ENST00000679773.1:n.2776C>T
ENST00000679926.1:n.4917C>T
ENST00000679999.1:c.*672C>T	ENSP00000505198.1:n.*672C>T
ENST00000680252.1:c.3282C>T
ENST00000680294.1:c.3408C>T	ENSP00000506113.1:p.Ile1136=
ENST00000680358.1:n.2914C>T
ENST00000680470.1:c.*1396C>T	ENSP00000505975.1:n.*1396C>T
ENST00000680554.1:c.*148C>T	ENSP00000505621.1:n.*148C>T
ENST00000680576.1:n.5091C>T
ENST00000680599.1:n.3656C>T
ENST00000680742.1:c.*148C>T	ENSP00000505206.1:n.*148C>T
ENST00000680791.1:n.2499C>T
ENST00000680885.1:n.5317C>T
ENST00000681158.1:c.3199C>T
ENST00000681203.1:c.3543C>T	ENSP00000506456.1:p.Ile1181=
ENST00000681371.1:n.3487C>T
ENST00000681425.1:n.4093C>T
ENST00000681639.1:n.1894C>T
ENST00000328194.7:c.3615C>T	ENSP00000328524.3:p.Ile1205=
ENST00000525784.5:c.551C>T
ENST00000527700.5:n.3177C>T
ENST00000528725.5:c.311C>T
ENST00000529977.5:n.1516C>T
ENST00000530044.5:c.3615C>T	ENSP00000435866.1:p.Ile1205=
ENST00000531747.1:c.851C>T
ENST00000533737.5:c.278C>T
NM_001243254.1:c.3615C>T	NP_001230183.1:p.Ile1205=
NM_015213.3:c.3615C>T	NP_056028.2:p.Ile1205=
XM_005252832.1:c.3615C>T	XP_005252889.1:p.Ile1205=
XM_011519952.1:c.3615C>T	XP_011518254.1:p.Ile1205=
XM_011519953.1:c.1713C>T	XP_011518255.1:p.Ile571=
XR_242782.2:n.3797C>T
XR_930851.1:n.3797C>T
NM_001348749.1:c.3543C>T	NP_001335678.1:p.Ile1181=
NM_001348750.1:c.3327C>T	NP_001335679.1:p.Ile1109=
NR_145966.2:n.3789C>T
NM_015213.4:c.3615C>T MANE Select	NP_056028.2:p.Ile1205=
NM_001243254.2:c.3615C>T	NP_001230183.1:p.Ile1205=
NM_001348749.2:c.3543C>T	NP_001335678.1:p.Ile1181=
NM_001348750.2:c.3327C>T	NP_001335679.1:p.Ile1109=