Canonical Allele Identifier: CA379597537

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163542G>T (hg19) ; chr11:g.9141995G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141995G>T , CM000673.2:g.9141995G>T	GRCh38
NC_000011.9:g.9163542G>T , CM000673.1:g.9163542G>T	GRCh37
NC_000011.8:g.9120118G>T	NCBI36
NG_053019.1:g.128341C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3625C>A MANE Select	ENSP00000328524.3:p.Pro1209Thr
ENST00000525784.6:n.1487C>A
ENST00000530780.2:c.*3451C>A	ENSP00000433925.1:n.*3451C>A
ENST00000531747.2:n.3296C>A
ENST00000679446.1:n.3546C>A
ENST00000679458.1:n.5026C>A
ENST00000679460.1:n.4687C>A
ENST00000679568.1:c.3625C>A	ENSP00000505860.1:p.Pro1209Thr
ENST00000679745.1:n.4130C>A
ENST00000679773.1:n.2786C>A
ENST00000679926.1:n.4927C>A
ENST00000679999.1:c.*682C>A	ENSP00000505198.1:n.*682C>A
ENST00000680252.1:c.3292C>A
ENST00000680294.1:c.3418C>A	ENSP00000506113.1:p.Pro1140Thr
ENST00000680358.1:n.2924C>A
ENST00000680470.1:c.*1406C>A	ENSP00000505975.1:n.*1406C>A
ENST00000680554.1:c.*158C>A	ENSP00000505621.1:n.*158C>A
ENST00000680576.1:n.5101C>A
ENST00000680599.1:n.3666C>A
ENST00000680742.1:c.*158C>A	ENSP00000505206.1:n.*158C>A
ENST00000680791.1:n.2509C>A
ENST00000680885.1:n.5327C>A
ENST00000681158.1:c.3209C>A
ENST00000681203.1:c.3553C>A	ENSP00000506456.1:p.Pro1185Thr
ENST00000681371.1:n.3497C>A
ENST00000681425.1:n.4103C>A
ENST00000681639.1:n.1904C>A
ENST00000328194.7:c.3625C>A	ENSP00000328524.3:p.Pro1209Thr
ENST00000525784.5:c.561C>A
ENST00000527700.5:n.3187C>A
ENST00000528725.5:c.321C>A
ENST00000529977.5:n.1526C>A
ENST00000530044.5:c.3625C>A	ENSP00000435866.1:p.Pro1209Thr
ENST00000531747.1:c.861C>A
ENST00000533737.5:c.288C>A
NM_001243254.1:c.3625C>A	NP_001230183.1:p.Pro1209Thr
NM_015213.3:c.3625C>A	NP_056028.2:p.Pro1209Thr
XM_005252832.1:c.3625C>A	XP_005252889.1:p.Pro1209Thr
XM_011519952.1:c.3625C>A	XP_011518254.1:p.Pro1209Thr
XM_011519953.1:c.1723C>A	XP_011518255.1:p.Pro575Thr
XR_242782.2:n.3807C>A
XR_930851.1:n.3807C>A
NM_001348749.1:c.3553C>A	NP_001335678.1:p.Pro1185Thr
NM_001348750.1:c.3337C>A	NP_001335679.1:p.Pro1113Thr
NR_145966.2:n.3799C>A
NM_015213.4:c.3625C>A MANE Select	NP_056028.2:p.Pro1209Thr
NM_001243254.2:c.3625C>A	NP_001230183.1:p.Pro1209Thr
NM_001348749.2:c.3553C>A	NP_001335678.1:p.Pro1185Thr
NM_001348750.2:c.3337C>A	NP_001335679.1:p.Pro1113Thr