Canonical Allele Identifier: CA379598045

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163613A>G (hg19) ; chr11:g.9142066A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142066A>G , CM000673.2:g.9142066A>G	GRCh38
NC_000011.9:g.9163613A>G , CM000673.1:g.9163613A>G	GRCh37
NC_000011.8:g.9120189A>G	NCBI36
NG_053019.1:g.128270T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3554T>C MANE Select	ENSP00000328524.3:p.Val1185Ala
ENST00000525784.6:n.1416T>C
ENST00000530780.2:c.*3380T>C	ENSP00000433925.1:n.*3380T>C
ENST00000531747.2:n.3225T>C
ENST00000679446.1:n.3475T>C
ENST00000679458.1:n.4955T>C
ENST00000679460.1:n.4616T>C
ENST00000679568.1:c.3554T>C	ENSP00000505860.1:p.Val1185Ala
ENST00000679745.1:n.4059T>C
ENST00000679773.1:n.2715T>C
ENST00000679926.1:n.4856T>C
ENST00000679999.1:c.*611T>C	ENSP00000505198.1:n.*611T>C
ENST00000680252.1:c.3221T>C
ENST00000680294.1:c.3347T>C	ENSP00000506113.1:p.Val1116Ala
ENST00000680358.1:n.2853T>C
ENST00000680470.1:c.*1335T>C	ENSP00000505975.1:n.*1335T>C
ENST00000680554.1:c.*87T>C	ENSP00000505621.1:n.*87T>C
ENST00000680576.1:n.5030T>C
ENST00000680599.1:n.3595T>C
ENST00000680742.1:c.*87T>C	ENSP00000505206.1:n.*87T>C
ENST00000680791.1:n.2438T>C
ENST00000680885.1:n.5256T>C
ENST00000681158.1:c.3138T>C
ENST00000681203.1:c.3482T>C	ENSP00000506456.1:p.Val1161Ala
ENST00000681371.1:n.3426T>C
ENST00000681425.1:n.4032T>C
ENST00000681639.1:n.1833T>C
ENST00000328194.7:c.3554T>C	ENSP00000328524.3:p.Val1185Ala
ENST00000525784.5:c.490T>C
ENST00000527700.5:n.3116T>C
ENST00000528725.5:c.250T>C
ENST00000529977.5:n.1455T>C
ENST00000530044.5:c.3554T>C	ENSP00000435866.1:p.Val1185Ala
ENST00000531747.1:c.790T>C
ENST00000533737.5:c.217T>C
NM_001243254.1:c.3554T>C	NP_001230183.1:p.Val1185Ala
NM_015213.3:c.3554T>C	NP_056028.2:p.Val1185Ala
XM_005252832.1:c.3554T>C	XP_005252889.1:p.Val1185Ala
XM_011519952.1:c.3554T>C	XP_011518254.1:p.Val1185Ala
XM_011519953.1:c.1652T>C	XP_011518255.1:p.Val551Ala
XR_242782.2:n.3736T>C
XR_930851.1:n.3736T>C
NM_001348749.1:c.3482T>C	NP_001335678.1:p.Val1161Ala
NM_001348750.1:c.3266T>C	NP_001335679.1:p.Val1089Ala
NR_145966.2:n.3728T>C
NM_015213.4:c.3554T>C MANE Select	NP_056028.2:p.Val1185Ala
NM_001243254.2:c.3554T>C	NP_001230183.1:p.Val1185Ala
NM_001348749.2:c.3482T>C	NP_001335678.1:p.Val1161Ala
NM_001348750.2:c.3266T>C	NP_001335679.1:p.Val1089Ala