Canonical Allele Identifier: CA379597540

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163544G>A (hg19) ; chr11:g.9141997G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141997G>A , CM000673.2:g.9141997G>A	GRCh38
NC_000011.9:g.9163544G>A , CM000673.1:g.9163544G>A	GRCh37
NC_000011.8:g.9120120G>A	NCBI36
NG_053019.1:g.128339C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3623C>T MANE Select	ENSP00000328524.3:p.Thr1208Ile
ENST00000525784.6:n.1485C>T
ENST00000530780.2:c.*3449C>T	ENSP00000433925.1:n.*3449C>T
ENST00000531747.2:n.3294C>T
ENST00000679446.1:n.3544C>T
ENST00000679458.1:n.5024C>T
ENST00000679460.1:n.4685C>T
ENST00000679568.1:c.3623C>T	ENSP00000505860.1:p.Thr1208Ile
ENST00000679745.1:n.4128C>T
ENST00000679773.1:n.2784C>T
ENST00000679926.1:n.4925C>T
ENST00000679999.1:c.*680C>T	ENSP00000505198.1:n.*680C>T
ENST00000680252.1:c.3290C>T
ENST00000680294.1:c.3416C>T	ENSP00000506113.1:p.Thr1139Ile
ENST00000680358.1:n.2922C>T
ENST00000680470.1:c.*1404C>T	ENSP00000505975.1:n.*1404C>T
ENST00000680554.1:c.*156C>T	ENSP00000505621.1:n.*156C>T
ENST00000680576.1:n.5099C>T
ENST00000680599.1:n.3664C>T
ENST00000680742.1:c.*156C>T	ENSP00000505206.1:n.*156C>T
ENST00000680791.1:n.2507C>T
ENST00000680885.1:n.5325C>T
ENST00000681158.1:c.3207C>T
ENST00000681203.1:c.3551C>T	ENSP00000506456.1:p.Thr1184Ile
ENST00000681371.1:n.3495C>T
ENST00000681425.1:n.4101C>T
ENST00000681639.1:n.1902C>T
ENST00000328194.7:c.3623C>T	ENSP00000328524.3:p.Thr1208Ile
ENST00000525784.5:c.559C>T
ENST00000527700.5:n.3185C>T
ENST00000528725.5:c.319C>T
ENST00000529977.5:n.1524C>T
ENST00000530044.5:c.3623C>T	ENSP00000435866.1:p.Thr1208Ile
ENST00000531747.1:c.859C>T
ENST00000533737.5:c.286C>T
NM_001243254.1:c.3623C>T	NP_001230183.1:p.Thr1208Ile
NM_015213.3:c.3623C>T	NP_056028.2:p.Thr1208Ile
XM_005252832.1:c.3623C>T	XP_005252889.1:p.Thr1208Ile
XM_011519952.1:c.3623C>T	XP_011518254.1:p.Thr1208Ile
XM_011519953.1:c.1721C>T	XP_011518255.1:p.Thr574Ile
XR_242782.2:n.3805C>T
XR_930851.1:n.3805C>T
NM_001348749.1:c.3551C>T	NP_001335678.1:p.Thr1184Ile
NM_001348750.1:c.3335C>T	NP_001335679.1:p.Thr1112Ile
NR_145966.2:n.3797C>T
NM_015213.4:c.3623C>T MANE Select	NP_056028.2:p.Thr1208Ile
NM_001243254.2:c.3623C>T	NP_001230183.1:p.Thr1208Ile
NM_001348749.2:c.3551C>T	NP_001335678.1:p.Thr1184Ile
NM_001348750.2:c.3335C>T	NP_001335679.1:p.Thr1112Ile