Canonical Allele Identifier: CA473040213

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163543A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141996A>G , CM000673.2:g.9141996A>G	GRCh38
NC_000011.9:g.9163543A>G , CM000673.1:g.9163543A>G	GRCh37
NC_000011.8:g.9120119A>G	NCBI36
NG_053019.1:g.128340T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3624T>C MANE Select	ENSP00000328524.3:p.Thr1208=
ENST00000525784.6:n.1486T>C
ENST00000530780.2:c.*3450T>C	ENSP00000433925.1:n.*3450T>C
ENST00000531747.2:n.3295T>C
ENST00000679446.1:n.3545T>C
ENST00000679458.1:n.5025T>C
ENST00000679460.1:n.4686T>C
ENST00000679568.1:c.3624T>C	ENSP00000505860.1:p.Thr1208=
ENST00000679745.1:n.4129T>C
ENST00000679773.1:n.2785T>C
ENST00000679926.1:n.4926T>C
ENST00000679999.1:c.*681T>C	ENSP00000505198.1:n.*681T>C
ENST00000680252.1:c.3291T>C
ENST00000680294.1:c.3417T>C	ENSP00000506113.1:p.Thr1139=
ENST00000680358.1:n.2923T>C
ENST00000680470.1:c.*1405T>C	ENSP00000505975.1:n.*1405T>C
ENST00000680554.1:c.*157T>C	ENSP00000505621.1:n.*157T>C
ENST00000680576.1:n.5100T>C
ENST00000680599.1:n.3665T>C
ENST00000680742.1:c.*157T>C	ENSP00000505206.1:n.*157T>C
ENST00000680791.1:n.2508T>C
ENST00000680885.1:n.5326T>C
ENST00000681158.1:c.3208T>C
ENST00000681203.1:c.3552T>C	ENSP00000506456.1:p.Thr1184=
ENST00000681371.1:n.3496T>C
ENST00000681425.1:n.4102T>C
ENST00000681639.1:n.1903T>C
ENST00000328194.7:c.3624T>C	ENSP00000328524.3:p.Thr1208=
ENST00000525784.5:c.560T>C
ENST00000527700.5:n.3186T>C
ENST00000528725.5:c.320T>C
ENST00000529977.5:n.1525T>C
ENST00000530044.5:c.3624T>C	ENSP00000435866.1:p.Thr1208=
ENST00000531747.1:c.860T>C
ENST00000533737.5:c.287T>C
NM_001243254.1:c.3624T>C	NP_001230183.1:p.Thr1208=
NM_015213.3:c.3624T>C	NP_056028.2:p.Thr1208=
XM_005252832.1:c.3624T>C	XP_005252889.1:p.Thr1208=
XM_011519952.1:c.3624T>C	XP_011518254.1:p.Thr1208=
XM_011519953.1:c.1722T>C	XP_011518255.1:p.Thr574=
XR_242782.2:n.3806T>C
XR_930851.1:n.3806T>C
NM_001348749.1:c.3552T>C	NP_001335678.1:p.Thr1184=
NM_001348750.1:c.3336T>C	NP_001335679.1:p.Thr1112=
NR_145966.2:n.3798T>C
NM_015213.4:c.3624T>C MANE Select	NP_056028.2:p.Thr1208=
NM_001243254.2:c.3624T>C	NP_001230183.1:p.Thr1208=
NM_001348749.2:c.3552T>C	NP_001335678.1:p.Thr1184=
NM_001348750.2:c.3336T>C	NP_001335679.1:p.Thr1112=