Canonical Allele Identifier: CA379597546

Gene: DENND5A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3623C>G MANE Select	ENSP00000328524.3:p.Thr1208Ser
ENST00000525784.6:n.1485C>G
ENST00000530780.2:c.*3449C>G	ENSP00000433925.1:n.*3449C>G
ENST00000531747.2:n.3294C>G
ENST00000679446.1:n.3544C>G
ENST00000679458.1:n.5024C>G
ENST00000679460.1:n.4685C>G
ENST00000679568.1:c.3623C>G	ENSP00000505860.1:p.Thr1208Ser
ENST00000679745.1:n.4128C>G
ENST00000679773.1:n.2784C>G
ENST00000679926.1:n.4925C>G
ENST00000679999.1:c.*680C>G	ENSP00000505198.1:n.*680C>G
ENST00000680252.1:c.3290C>G
ENST00000680294.1:c.3416C>G	ENSP00000506113.1:p.Thr1139Ser
ENST00000680358.1:n.2922C>G
ENST00000680470.1:c.*1404C>G	ENSP00000505975.1:n.*1404C>G
ENST00000680554.1:c.*156C>G	ENSP00000505621.1:n.*156C>G
ENST00000680576.1:n.5099C>G
ENST00000680599.1:n.3664C>G
ENST00000680742.1:c.*156C>G	ENSP00000505206.1:n.*156C>G
ENST00000680791.1:n.2507C>G
ENST00000680885.1:n.5325C>G
ENST00000681158.1:c.3207C>G
ENST00000681203.1:c.3551C>G	ENSP00000506456.1:p.Thr1184Ser
ENST00000681371.1:n.3495C>G
ENST00000681425.1:n.4101C>G
ENST00000681639.1:n.1902C>G
ENST00000328194.7:c.3623C>G	ENSP00000328524.3:p.Thr1208Ser
ENST00000525784.5:c.559C>G
ENST00000527700.5:n.3185C>G
ENST00000528725.5:c.319C>G
ENST00000529977.5:n.1524C>G
ENST00000530044.5:c.3623C>G	ENSP00000435866.1:p.Thr1208Ser
ENST00000531747.1:c.859C>G
ENST00000533737.5:c.286C>G
NM_001243254.1:c.3623C>G	NP_001230183.1:p.Thr1208Ser
NM_015213.3:c.3623C>G	NP_056028.2:p.Thr1208Ser
XM_005252832.1:c.3623C>G	XP_005252889.1:p.Thr1208Ser
XM_011519952.1:c.3623C>G	XP_011518254.1:p.Thr1208Ser
XM_011519953.1:c.1721C>G	XP_011518255.1:p.Thr574Ser
XR_242782.2:n.3805C>G
XR_930851.1:n.3805C>G
NM_001348749.1:c.3551C>G	NP_001335678.1:p.Thr1184Ser
NM_001348750.1:c.3335C>G	NP_001335679.1:p.Thr1112Ser
NR_145966.2:n.3797C>G
NM_015213.4:c.3623C>G MANE Select	NP_056028.2:p.Thr1208Ser
NM_001243254.2:c.3623C>G	NP_001230183.1:p.Thr1208Ser
NM_001348749.2:c.3551C>G	NP_001335678.1:p.Thr1184Ser
NM_001348750.2:c.3335C>G	NP_001335679.1:p.Thr1112Ser