Canonical Allele Identifier: CA379597112

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163493C>A (hg19) ; chr11:g.9141946C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141946C>A , CM000673.2:g.9141946C>A	GRCh38
NC_000011.9:g.9163493C>A , CM000673.1:g.9163493C>A	GRCh37
NC_000011.8:g.9120069C>A	NCBI36
NG_053019.1:g.128390G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3674G>T MANE Select	ENSP00000328524.3:p.Gly1225Val
ENST00000525784.6:n.1536G>T
ENST00000530780.2:c.*3500G>T	ENSP00000433925.1:n.*3500G>T
ENST00000531747.2:n.3345G>T
ENST00000679446.1:n.3595G>T
ENST00000679458.1:n.5075G>T
ENST00000679460.1:n.4736G>T
ENST00000679568.1:c.3674G>T	ENSP00000505860.1:p.Gly1225Val
ENST00000679745.1:n.4179G>T
ENST00000679773.1:n.2835G>T
ENST00000679926.1:n.4976G>T
ENST00000679999.1:c.*731G>T	ENSP00000505198.1:n.*731G>T
ENST00000680252.1:c.3341G>T
ENST00000680294.1:c.3467G>T	ENSP00000506113.1:p.Gly1156Val
ENST00000680358.1:n.2973G>T
ENST00000680470.1:c.*1455G>T	ENSP00000505975.1:n.*1455G>T
ENST00000680554.1:c.*207G>T	ENSP00000505621.1:n.*207G>T
ENST00000680576.1:n.5150G>T
ENST00000680599.1:n.3715G>T
ENST00000680742.1:c.*179+28G>T	ENSP00000505206.1:n.*179+28G>T
ENST00000680791.1:n.2558G>T
ENST00000680885.1:n.5376G>T
ENST00000681158.1:c.3258G>T
ENST00000681203.1:c.3602G>T	ENSP00000506456.1:p.Gly1201Val
ENST00000681371.1:n.3546G>T
ENST00000681425.1:n.4152G>T
ENST00000681639.1:n.1953G>T
ENST00000328194.7:c.3674G>T	ENSP00000328524.3:p.Gly1225Val
ENST00000525784.5:c.610G>T
ENST00000527700.5:n.3236G>T
ENST00000528725.5:c.370G>T
ENST00000529977.5:n.1575G>T
ENST00000530044.5:c.3646+28G>T	ENSP00000435866.1:n.3646+28G>T
ENST00000531747.1:c.910G>T
ENST00000533737.5:c.337G>T
NM_001243254.1:c.3646+28G>T	NP_001230183.1:n.3646+28G>T
NM_015213.3:c.3674G>T	NP_056028.2:p.Gly1225Val
XM_005252832.1:c.3674G>T	XP_005252889.1:p.Gly1225Val
XM_011519952.1:c.3646+28G>T	XP_011518254.1:n.3646+28G>T
XM_011519953.1:c.1772G>T	XP_011518255.1:p.Gly591Val
XR_242782.2:n.3856G>T
XR_930851.1:n.3828+28G>T
NM_001348749.1:c.3602G>T	NP_001335678.1:p.Gly1201Val
NM_001348750.1:c.3386G>T	NP_001335679.1:p.Gly1129Val
NR_145966.2:n.3848G>T
NM_015213.4:c.3674G>T MANE Select	NP_056028.2:p.Gly1225Val
NM_001243254.2:c.3646+28G>T	NP_001230183.1:n.3646+28G>T
NM_001348749.2:c.3602G>T	NP_001335678.1:p.Gly1201Val
NM_001348750.2:c.3386G>T	NP_001335679.1:p.Gly1129Val