Canonical Allele Identifier: CA379597280

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163517T>A (hg19) ; chr11:g.9141970T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141970T>A , CM000673.2:g.9141970T>A	GRCh38
NC_000011.9:g.9163517T>A , CM000673.1:g.9163517T>A	GRCh37
NC_000011.8:g.9120093T>A	NCBI36
NG_053019.1:g.128366A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3650A>T MANE Select	ENSP00000328524.3:p.Lys1217Met
ENST00000525784.6:n.1512A>T
ENST00000530780.2:c.*3476A>T	ENSP00000433925.1:n.*3476A>T
ENST00000531747.2:n.3321A>T
ENST00000679446.1:n.3571A>T
ENST00000679458.1:n.5051A>T
ENST00000679460.1:n.4712A>T
ENST00000679568.1:c.3650A>T	ENSP00000505860.1:p.Lys1217Met
ENST00000679745.1:n.4155A>T
ENST00000679773.1:n.2811A>T
ENST00000679926.1:n.4952A>T
ENST00000679999.1:c.*707A>T	ENSP00000505198.1:n.*707A>T
ENST00000680252.1:c.3317A>T
ENST00000680294.1:c.3443A>T	ENSP00000506113.1:p.Lys1148Met
ENST00000680358.1:n.2949A>T
ENST00000680470.1:c.*1431A>T	ENSP00000505975.1:n.*1431A>T
ENST00000680554.1:c.*183A>T	ENSP00000505621.1:n.*183A>T
ENST00000680576.1:n.5126A>T
ENST00000680599.1:n.3691A>T
ENST00000680742.1:c.*179+4A>T	ENSP00000505206.1:n.*179+4A>T
ENST00000680791.1:n.2534A>T
ENST00000680885.1:n.5352A>T
ENST00000681158.1:c.3234A>T
ENST00000681203.1:c.3578A>T	ENSP00000506456.1:p.Lys1193Met
ENST00000681371.1:n.3522A>T
ENST00000681425.1:n.4128A>T
ENST00000681639.1:n.1929A>T
ENST00000328194.7:c.3650A>T	ENSP00000328524.3:p.Lys1217Met
ENST00000525784.5:c.586A>T
ENST00000527700.5:n.3212A>T
ENST00000528725.5:c.346A>T
ENST00000529977.5:n.1551A>T
ENST00000530044.5:c.3646+4A>T	ENSP00000435866.1:n.3646+4A>T
ENST00000531747.1:c.886A>T
ENST00000533737.5:c.313A>T
NM_001243254.1:c.3646+4A>T	NP_001230183.1:n.3646+4A>T
NM_015213.3:c.3650A>T	NP_056028.2:p.Lys1217Met
XM_005252832.1:c.3650A>T	XP_005252889.1:p.Lys1217Met
XM_011519952.1:c.3646+4A>T	XP_011518254.1:n.3646+4A>T
XM_011519953.1:c.1748A>T	XP_011518255.1:p.Lys583Met
XR_242782.2:n.3832A>T
XR_930851.1:n.3828+4A>T
NM_001348749.1:c.3578A>T	NP_001335678.1:p.Lys1193Met
NM_001348750.1:c.3362A>T	NP_001335679.1:p.Lys1121Met
NR_145966.2:n.3824A>T
NM_015213.4:c.3650A>T MANE Select	NP_056028.2:p.Lys1217Met
NM_001243254.2:c.3646+4A>T	NP_001230183.1:n.3646+4A>T
NM_001348749.2:c.3578A>T	NP_001335678.1:p.Lys1193Met
NM_001348750.2:c.3362A>T	NP_001335679.1:p.Lys1121Met