Canonical Allele Identifier: CA473040228

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163564A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142017A>G , CM000673.2:g.9142017A>G	GRCh38
NC_000011.9:g.9163564A>G , CM000673.1:g.9163564A>G	GRCh37
NC_000011.8:g.9120140A>G	NCBI36
NG_053019.1:g.128319T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3603T>C MANE Select	ENSP00000328524.3:p.Phe1201=
ENST00000525784.6:n.1465T>C
ENST00000530780.2:c.*3429T>C	ENSP00000433925.1:n.*3429T>C
ENST00000531747.2:n.3274T>C
ENST00000679446.1:n.3524T>C
ENST00000679458.1:n.5004T>C
ENST00000679460.1:n.4665T>C
ENST00000679568.1:c.3603T>C	ENSP00000505860.1:p.Phe1201=
ENST00000679745.1:n.4108T>C
ENST00000679773.1:n.2764T>C
ENST00000679926.1:n.4905T>C
ENST00000679999.1:c.*660T>C	ENSP00000505198.1:n.*660T>C
ENST00000680252.1:c.3270T>C
ENST00000680294.1:c.3396T>C	ENSP00000506113.1:p.Phe1132=
ENST00000680358.1:n.2902T>C
ENST00000680470.1:c.*1384T>C	ENSP00000505975.1:n.*1384T>C
ENST00000680554.1:c.*136T>C	ENSP00000505621.1:n.*136T>C
ENST00000680576.1:n.5079T>C
ENST00000680599.1:n.3644T>C
ENST00000680742.1:c.*136T>C	ENSP00000505206.1:n.*136T>C
ENST00000680791.1:n.2487T>C
ENST00000680885.1:n.5305T>C
ENST00000681158.1:c.3187T>C
ENST00000681203.1:c.3531T>C	ENSP00000506456.1:p.Phe1177=
ENST00000681371.1:n.3475T>C
ENST00000681425.1:n.4081T>C
ENST00000681639.1:n.1882T>C
ENST00000328194.7:c.3603T>C	ENSP00000328524.3:p.Phe1201=
ENST00000525784.5:c.539T>C
ENST00000527700.5:n.3165T>C
ENST00000528725.5:c.299T>C
ENST00000529977.5:n.1504T>C
ENST00000530044.5:c.3603T>C	ENSP00000435866.1:p.Phe1201=
ENST00000531747.1:c.839T>C
ENST00000533737.5:c.266T>C
NM_001243254.1:c.3603T>C	NP_001230183.1:p.Phe1201=
NM_015213.3:c.3603T>C	NP_056028.2:p.Phe1201=
XM_005252832.1:c.3603T>C	XP_005252889.1:p.Phe1201=
XM_011519952.1:c.3603T>C	XP_011518254.1:p.Phe1201=
XM_011519953.1:c.1701T>C	XP_011518255.1:p.Phe567=
XR_242782.2:n.3785T>C
XR_930851.1:n.3785T>C
NM_001348749.1:c.3531T>C	NP_001335678.1:p.Phe1177=
NM_001348750.1:c.3315T>C	NP_001335679.1:p.Phe1105=
NR_145966.2:n.3777T>C
NM_015213.4:c.3603T>C MANE Select	NP_056028.2:p.Phe1201=
NM_001243254.2:c.3603T>C	NP_001230183.1:p.Phe1201=
NM_001348749.2:c.3531T>C	NP_001335678.1:p.Phe1177=
NM_001348750.2:c.3315T>C	NP_001335679.1:p.Phe1105=