Canonical Allele Identifier: CA379597747

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163575A>C (hg19) ; chr11:g.9142028A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142028A>C , CM000673.2:g.9142028A>C	GRCh38
NC_000011.9:g.9163575A>C , CM000673.1:g.9163575A>C	GRCh37
NC_000011.8:g.9120151A>C	NCBI36
NG_053019.1:g.128308T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3592T>G MANE Select	ENSP00000328524.3:p.Phe1198Val
ENST00000525784.6:n.1454T>G
ENST00000530780.2:c.*3418T>G	ENSP00000433925.1:n.*3418T>G
ENST00000531747.2:n.3263T>G
ENST00000679446.1:n.3513T>G
ENST00000679458.1:n.4993T>G
ENST00000679460.1:n.4654T>G
ENST00000679568.1:c.3592T>G	ENSP00000505860.1:p.Phe1198Val
ENST00000679745.1:n.4097T>G
ENST00000679773.1:n.2753T>G
ENST00000679926.1:n.4894T>G
ENST00000679999.1:c.*649T>G	ENSP00000505198.1:n.*649T>G
ENST00000680252.1:c.3259T>G
ENST00000680294.1:c.3385T>G	ENSP00000506113.1:p.Phe1129Val
ENST00000680358.1:n.2891T>G
ENST00000680470.1:c.*1373T>G	ENSP00000505975.1:n.*1373T>G
ENST00000680554.1:c.*125T>G	ENSP00000505621.1:n.*125T>G
ENST00000680576.1:n.5068T>G
ENST00000680599.1:n.3633T>G
ENST00000680742.1:c.*125T>G	ENSP00000505206.1:n.*125T>G
ENST00000680791.1:n.2476T>G
ENST00000680885.1:n.5294T>G
ENST00000681158.1:c.3176T>G
ENST00000681203.1:c.3520T>G	ENSP00000506456.1:p.Phe1174Val
ENST00000681371.1:n.3464T>G
ENST00000681425.1:n.4070T>G
ENST00000681639.1:n.1871T>G
ENST00000328194.7:c.3592T>G	ENSP00000328524.3:p.Phe1198Val
ENST00000525784.5:c.528T>G
ENST00000527700.5:n.3154T>G
ENST00000528725.5:c.288T>G
ENST00000529977.5:n.1493T>G
ENST00000530044.5:c.3592T>G	ENSP00000435866.1:p.Phe1198Val
ENST00000531747.1:c.828T>G
ENST00000533737.5:c.255T>G
NM_001243254.1:c.3592T>G	NP_001230183.1:p.Phe1198Val
NM_015213.3:c.3592T>G	NP_056028.2:p.Phe1198Val
XM_005252832.1:c.3592T>G	XP_005252889.1:p.Phe1198Val
XM_011519952.1:c.3592T>G	XP_011518254.1:p.Phe1198Val
XM_011519953.1:c.1690T>G	XP_011518255.1:p.Phe564Val
XR_242782.2:n.3774T>G
XR_930851.1:n.3774T>G
NM_001348749.1:c.3520T>G	NP_001335678.1:p.Phe1174Val
NM_001348750.1:c.3304T>G	NP_001335679.1:p.Phe1102Val
NR_145966.2:n.3766T>G
NM_015213.4:c.3592T>G MANE Select	NP_056028.2:p.Phe1198Val
NM_001243254.2:c.3592T>G	NP_001230183.1:p.Phe1198Val
NM_001348749.2:c.3520T>G	NP_001335678.1:p.Phe1174Val
NM_001348750.2:c.3304T>G	NP_001335679.1:p.Phe1102Val