Canonical Allele Identifier: CA379598267

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163652T>A (hg19) ; chr11:g.9142105T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142105T>A , CM000673.2:g.9142105T>A	GRCh38
NC_000011.9:g.9163652T>A , CM000673.1:g.9163652T>A	GRCh37
NC_000011.8:g.9120228T>A	NCBI36
NG_053019.1:g.128231A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3515A>T MANE Select	ENSP00000328524.3:p.Lys1172Ile
ENST00000525784.6:n.1377A>T
ENST00000530780.2:c.*3341A>T	ENSP00000433925.1:n.*3341A>T
ENST00000531747.2:n.3186A>T
ENST00000679446.1:n.3436A>T
ENST00000679458.1:n.4916A>T
ENST00000679460.1:n.4577A>T
ENST00000679568.1:c.3515A>T	ENSP00000505860.1:p.Lys1172Ile
ENST00000679745.1:n.4020A>T
ENST00000679773.1:n.2676A>T
ENST00000679926.1:n.4817A>T
ENST00000679999.1:c.*572A>T	ENSP00000505198.1:n.*572A>T
ENST00000680252.1:c.3182A>T
ENST00000680294.1:c.3308A>T	ENSP00000506113.1:p.Lys1103Ile
ENST00000680358.1:n.2814A>T
ENST00000680470.1:c.*1296A>T	ENSP00000505975.1:n.*1296A>T
ENST00000680554.1:c.*48A>T	ENSP00000505621.1:n.*48A>T
ENST00000680576.1:n.4991A>T
ENST00000680599.1:n.3556A>T
ENST00000680742.1:c.*48A>T	ENSP00000505206.1:n.*48A>T
ENST00000680791.1:n.2399A>T
ENST00000680885.1:n.5217A>T
ENST00000681158.1:c.3099A>T
ENST00000681203.1:c.3443A>T	ENSP00000506456.1:p.Lys1148Ile
ENST00000681371.1:n.3387A>T
ENST00000681425.1:n.3993A>T
ENST00000681639.1:n.1794A>T
ENST00000328194.7:c.3515A>T	ENSP00000328524.3:p.Lys1172Ile
ENST00000525784.5:c.451A>T
ENST00000527700.5:n.3077A>T
ENST00000528725.5:c.211A>T
ENST00000529977.5:n.1416A>T
ENST00000530044.5:c.3515A>T	ENSP00000435866.1:p.Lys1172Ile
ENST00000531747.1:c.751A>T
ENST00000533737.5:c.178A>T
NM_001243254.1:c.3515A>T	NP_001230183.1:p.Lys1172Ile
NM_015213.3:c.3515A>T	NP_056028.2:p.Lys1172Ile
XM_005252832.1:c.3515A>T	XP_005252889.1:p.Lys1172Ile
XM_011519952.1:c.3515A>T	XP_011518254.1:p.Lys1172Ile
XM_011519953.1:c.1613A>T	XP_011518255.1:p.Lys538Ile
XR_242782.2:n.3697A>T
XR_930851.1:n.3697A>T
NM_001348749.1:c.3443A>T	NP_001335678.1:p.Lys1148Ile
NM_001348750.1:c.3227A>T	NP_001335679.1:p.Lys1076Ile
NR_145966.2:n.3689A>T
NM_015213.4:c.3515A>T MANE Select	NP_056028.2:p.Lys1172Ile
NM_001243254.2:c.3515A>T	NP_001230183.1:p.Lys1172Ile
NM_001348749.2:c.3443A>T	NP_001335678.1:p.Lys1148Ile
NM_001348750.2:c.3227A>T	NP_001335679.1:p.Lys1076Ile