Canonical Allele Identifier: CA379597817

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163585T>A (hg19) ; chr11:g.9142038T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142038T>A , CM000673.2:g.9142038T>A	GRCh38
NC_000011.9:g.9163585T>A , CM000673.1:g.9163585T>A	GRCh37
NC_000011.8:g.9120161T>A	NCBI36
NG_053019.1:g.128298A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3582A>T MANE Select	ENSP00000328524.3:p.Arg1194Ser
ENST00000525784.6:n.1444A>T
ENST00000530780.2:c.*3408A>T	ENSP00000433925.1:n.*3408A>T
ENST00000531747.2:n.3253A>T
ENST00000679446.1:n.3503A>T
ENST00000679458.1:n.4983A>T
ENST00000679460.1:n.4644A>T
ENST00000679568.1:c.3582A>T	ENSP00000505860.1:p.Arg1194Ser
ENST00000679745.1:n.4087A>T
ENST00000679773.1:n.2743A>T
ENST00000679926.1:n.4884A>T
ENST00000679999.1:c.*639A>T	ENSP00000505198.1:n.*639A>T
ENST00000680252.1:c.3249A>T
ENST00000680294.1:c.3375A>T	ENSP00000506113.1:p.Arg1125Ser
ENST00000680358.1:n.2881A>T
ENST00000680470.1:c.*1363A>T	ENSP00000505975.1:n.*1363A>T
ENST00000680554.1:c.*115A>T	ENSP00000505621.1:n.*115A>T
ENST00000680576.1:n.5058A>T
ENST00000680599.1:n.3623A>T
ENST00000680742.1:c.*115A>T	ENSP00000505206.1:n.*115A>T
ENST00000680791.1:n.2466A>T
ENST00000680885.1:n.5284A>T
ENST00000681158.1:c.3166A>T
ENST00000681203.1:c.3510A>T	ENSP00000506456.1:p.Arg1170Ser
ENST00000681371.1:n.3454A>T
ENST00000681425.1:n.4060A>T
ENST00000681639.1:n.1861A>T
ENST00000328194.7:c.3582A>T	ENSP00000328524.3:p.Arg1194Ser
ENST00000525784.5:c.518A>T
ENST00000527700.5:n.3144A>T
ENST00000528725.5:c.278A>T
ENST00000529977.5:n.1483A>T
ENST00000530044.5:c.3582A>T	ENSP00000435866.1:p.Arg1194Ser
ENST00000531747.1:c.818A>T
ENST00000533737.5:c.245A>T
NM_001243254.1:c.3582A>T	NP_001230183.1:p.Arg1194Ser
NM_015213.3:c.3582A>T	NP_056028.2:p.Arg1194Ser
XM_005252832.1:c.3582A>T	XP_005252889.1:p.Arg1194Ser
XM_011519952.1:c.3582A>T	XP_011518254.1:p.Arg1194Ser
XM_011519953.1:c.1680A>T	XP_011518255.1:p.Arg560Ser
XR_242782.2:n.3764A>T
XR_930851.1:n.3764A>T
NM_001348749.1:c.3510A>T	NP_001335678.1:p.Arg1170Ser
NM_001348750.1:c.3294A>T	NP_001335679.1:p.Arg1098Ser
NR_145966.2:n.3756A>T
NM_015213.4:c.3582A>T MANE Select	NP_056028.2:p.Arg1194Ser
NM_001243254.2:c.3582A>T	NP_001230183.1:p.Arg1194Ser
NM_001348749.2:c.3510A>T	NP_001335678.1:p.Arg1170Ser
NM_001348750.2:c.3294A>T	NP_001335679.1:p.Arg1098Ser