Canonical Allele Identifier: CA473040236

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163579C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142032C>G , CM000673.2:g.9142032C>G	GRCh38
NC_000011.9:g.9163579C>G , CM000673.1:g.9163579C>G	GRCh37
NC_000011.8:g.9120155C>G	NCBI36
NG_053019.1:g.128304G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3588G>C MANE Select	ENSP00000328524.3:p.Arg1196=
ENST00000525784.6:n.1450G>C
ENST00000530780.2:c.*3414G>C	ENSP00000433925.1:n.*3414G>C
ENST00000531747.2:n.3259G>C
ENST00000679446.1:n.3509G>C
ENST00000679458.1:n.4989G>C
ENST00000679460.1:n.4650G>C
ENST00000679568.1:c.3588G>C	ENSP00000505860.1:p.Arg1196=
ENST00000679745.1:n.4093G>C
ENST00000679773.1:n.2749G>C
ENST00000679926.1:n.4890G>C
ENST00000679999.1:c.*645G>C	ENSP00000505198.1:n.*645G>C
ENST00000680252.1:c.3255G>C
ENST00000680294.1:c.3381G>C	ENSP00000506113.1:p.Arg1127=
ENST00000680358.1:n.2887G>C
ENST00000680470.1:c.*1369G>C	ENSP00000505975.1:n.*1369G>C
ENST00000680554.1:c.*121G>C	ENSP00000505621.1:n.*121G>C
ENST00000680576.1:n.5064G>C
ENST00000680599.1:n.3629G>C
ENST00000680742.1:c.*121G>C	ENSP00000505206.1:n.*121G>C
ENST00000680791.1:n.2472G>C
ENST00000680885.1:n.5290G>C
ENST00000681158.1:c.3172G>C
ENST00000681203.1:c.3516G>C	ENSP00000506456.1:p.Arg1172=
ENST00000681371.1:n.3460G>C
ENST00000681425.1:n.4066G>C
ENST00000681639.1:n.1867G>C
ENST00000328194.7:c.3588G>C	ENSP00000328524.3:p.Arg1196=
ENST00000525784.5:c.524G>C
ENST00000527700.5:n.3150G>C
ENST00000528725.5:c.284G>C
ENST00000529977.5:n.1489G>C
ENST00000530044.5:c.3588G>C	ENSP00000435866.1:p.Arg1196=
ENST00000531747.1:c.824G>C
ENST00000533737.5:c.251G>C
NM_001243254.1:c.3588G>C	NP_001230183.1:p.Arg1196=
NM_015213.3:c.3588G>C	NP_056028.2:p.Arg1196=
XM_005252832.1:c.3588G>C	XP_005252889.1:p.Arg1196=
XM_011519952.1:c.3588G>C	XP_011518254.1:p.Arg1196=
XM_011519953.1:c.1686G>C	XP_011518255.1:p.Arg562=
XR_242782.2:n.3770G>C
XR_930851.1:n.3770G>C
NM_001348749.1:c.3516G>C	NP_001335678.1:p.Arg1172=
NM_001348750.1:c.3300G>C	NP_001335679.1:p.Arg1100=
NR_145966.2:n.3762G>C
NM_015213.4:c.3588G>C MANE Select	NP_056028.2:p.Arg1196=
NM_001243254.2:c.3588G>C	NP_001230183.1:p.Arg1196=
NM_001348749.2:c.3516G>C	NP_001335678.1:p.Arg1172=
NM_001348750.2:c.3300G>C	NP_001335679.1:p.Arg1100=