Canonical Allele Identifier: CA379597435

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163533T>G (hg19) ; chr11:g.9141986T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141986T>G , CM000673.2:g.9141986T>G	GRCh38
NC_000011.9:g.9163533T>G , CM000673.1:g.9163533T>G	GRCh37
NC_000011.8:g.9120109T>G	NCBI36
NG_053019.1:g.128350A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3634A>C MANE Select	ENSP00000328524.3:p.Ile1212Leu
ENST00000525784.6:n.1496A>C
ENST00000530780.2:c.*3460A>C	ENSP00000433925.1:n.*3460A>C
ENST00000531747.2:n.3305A>C
ENST00000679446.1:n.3555A>C
ENST00000679458.1:n.5035A>C
ENST00000679460.1:n.4696A>C
ENST00000679568.1:c.3634A>C	ENSP00000505860.1:p.Ile1212Leu
ENST00000679745.1:n.4139A>C
ENST00000679773.1:n.2795A>C
ENST00000679926.1:n.4936A>C
ENST00000679999.1:c.*691A>C	ENSP00000505198.1:n.*691A>C
ENST00000680252.1:c.3301A>C
ENST00000680294.1:c.3427A>C	ENSP00000506113.1:p.Ile1143Leu
ENST00000680358.1:n.2933A>C
ENST00000680470.1:c.*1415A>C	ENSP00000505975.1:n.*1415A>C
ENST00000680554.1:c.*167A>C	ENSP00000505621.1:n.*167A>C
ENST00000680576.1:n.5110A>C
ENST00000680599.1:n.3675A>C
ENST00000680742.1:c.*167A>C	ENSP00000505206.1:n.*167A>C
ENST00000680791.1:n.2518A>C
ENST00000680885.1:n.5336A>C
ENST00000681158.1:c.3218A>C
ENST00000681203.1:c.3562A>C	ENSP00000506456.1:p.Ile1188Leu
ENST00000681371.1:n.3506A>C
ENST00000681425.1:n.4112A>C
ENST00000681639.1:n.1913A>C
ENST00000328194.7:c.3634A>C	ENSP00000328524.3:p.Ile1212Leu
ENST00000525784.5:c.570A>C
ENST00000527700.5:n.3196A>C
ENST00000528725.5:c.330A>C
ENST00000529977.5:n.1535A>C
ENST00000530044.5:c.3634A>C	ENSP00000435866.1:p.Ile1212Leu
ENST00000531747.1:c.870A>C
ENST00000533737.5:c.297A>C
NM_001243254.1:c.3634A>C	NP_001230183.1:p.Ile1212Leu
NM_015213.3:c.3634A>C	NP_056028.2:p.Ile1212Leu
XM_005252832.1:c.3634A>C	XP_005252889.1:p.Ile1212Leu
XM_011519952.1:c.3634A>C	XP_011518254.1:p.Ile1212Leu
XM_011519953.1:c.1732A>C	XP_011518255.1:p.Ile578Leu
XR_242782.2:n.3816A>C
XR_930851.1:n.3816A>C
NM_001348749.1:c.3562A>C	NP_001335678.1:p.Ile1188Leu
NM_001348750.1:c.3346A>C	NP_001335679.1:p.Ile1116Leu
NR_145966.2:n.3808A>C
NM_015213.4:c.3634A>C MANE Select	NP_056028.2:p.Ile1212Leu
NM_001243254.2:c.3634A>C	NP_001230183.1:p.Ile1212Leu
NM_001348749.2:c.3562A>C	NP_001335678.1:p.Ile1188Leu
NM_001348750.2:c.3346A>C	NP_001335679.1:p.Ile1116Leu