Canonical Allele Identifier: CA379597360

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163526T>A (hg19) ; chr11:g.9141979T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141979T>A , CM000673.2:g.9141979T>A	GRCh38
NC_000011.9:g.9163526T>A , CM000673.1:g.9163526T>A	GRCh37
NC_000011.8:g.9120102T>A	NCBI36
NG_053019.1:g.128357A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3641A>T MANE Select	ENSP00000328524.3:p.Lys1214Met
ENST00000525784.6:n.1503A>T
ENST00000530780.2:c.*3467A>T	ENSP00000433925.1:n.*3467A>T
ENST00000531747.2:n.3312A>T
ENST00000679446.1:n.3562A>T
ENST00000679458.1:n.5042A>T
ENST00000679460.1:n.4703A>T
ENST00000679568.1:c.3641A>T	ENSP00000505860.1:p.Lys1214Met
ENST00000679745.1:n.4146A>T
ENST00000679773.1:n.2802A>T
ENST00000679926.1:n.4943A>T
ENST00000679999.1:c.*698A>T	ENSP00000505198.1:n.*698A>T
ENST00000680252.1:c.3308A>T
ENST00000680294.1:c.3434A>T	ENSP00000506113.1:p.Lys1145Met
ENST00000680358.1:n.2940A>T
ENST00000680470.1:c.*1422A>T	ENSP00000505975.1:n.*1422A>T
ENST00000680554.1:c.*174A>T	ENSP00000505621.1:n.*174A>T
ENST00000680576.1:n.5117A>T
ENST00000680599.1:n.3682A>T
ENST00000680742.1:c.*174A>T	ENSP00000505206.1:n.*174A>T
ENST00000680791.1:n.2525A>T
ENST00000680885.1:n.5343A>T
ENST00000681158.1:c.3225A>T
ENST00000681203.1:c.3569A>T	ENSP00000506456.1:p.Lys1190Met
ENST00000681371.1:n.3513A>T
ENST00000681425.1:n.4119A>T
ENST00000681639.1:n.1920A>T
ENST00000328194.7:c.3641A>T	ENSP00000328524.3:p.Lys1214Met
ENST00000525784.5:c.577A>T
ENST00000527700.5:n.3203A>T
ENST00000528725.5:c.337A>T
ENST00000529977.5:n.1542A>T
ENST00000530044.5:c.3641A>T	ENSP00000435866.1:p.Lys1214Met
ENST00000531747.1:c.877A>T
ENST00000533737.5:c.304A>T
NM_001243254.1:c.3641A>T	NP_001230183.1:p.Lys1214Met
NM_015213.3:c.3641A>T	NP_056028.2:p.Lys1214Met
XM_005252832.1:c.3641A>T	XP_005252889.1:p.Lys1214Met
XM_011519952.1:c.3641A>T	XP_011518254.1:p.Lys1214Met
XM_011519953.1:c.1739A>T	XP_011518255.1:p.Lys580Met
XR_242782.2:n.3823A>T
XR_930851.1:n.3823A>T
NM_001348749.1:c.3569A>T	NP_001335678.1:p.Lys1190Met
NM_001348750.1:c.3353A>T	NP_001335679.1:p.Lys1118Met
NR_145966.2:n.3815A>T
NM_015213.4:c.3641A>T MANE Select	NP_056028.2:p.Lys1214Met
NM_001243254.2:c.3641A>T	NP_001230183.1:p.Lys1214Met
NM_001348749.2:c.3569A>T	NP_001335678.1:p.Lys1190Met
NM_001348750.2:c.3353A>T	NP_001335679.1:p.Lys1118Met