Canonical Allele Identifier: CA379597723

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163572A>G (hg19) ; chr11:g.9142025A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142025A>G , CM000673.2:g.9142025A>G	GRCh38
NC_000011.9:g.9163572A>G , CM000673.1:g.9163572A>G	GRCh37
NC_000011.8:g.9120148A>G	NCBI36
NG_053019.1:g.128311T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3595T>C MANE Select	ENSP00000328524.3:p.Cys1199Arg
ENST00000525784.6:n.1457T>C
ENST00000530780.2:c.*3421T>C	ENSP00000433925.1:n.*3421T>C
ENST00000531747.2:n.3266T>C
ENST00000679446.1:n.3516T>C
ENST00000679458.1:n.4996T>C
ENST00000679460.1:n.4657T>C
ENST00000679568.1:c.3595T>C	ENSP00000505860.1:p.Cys1199Arg
ENST00000679745.1:n.4100T>C
ENST00000679773.1:n.2756T>C
ENST00000679926.1:n.4897T>C
ENST00000679999.1:c.*652T>C	ENSP00000505198.1:n.*652T>C
ENST00000680252.1:c.3262T>C
ENST00000680294.1:c.3388T>C	ENSP00000506113.1:p.Cys1130Arg
ENST00000680358.1:n.2894T>C
ENST00000680470.1:c.*1376T>C	ENSP00000505975.1:n.*1376T>C
ENST00000680554.1:c.*128T>C	ENSP00000505621.1:n.*128T>C
ENST00000680576.1:n.5071T>C
ENST00000680599.1:n.3636T>C
ENST00000680742.1:c.*128T>C	ENSP00000505206.1:n.*128T>C
ENST00000680791.1:n.2479T>C
ENST00000680885.1:n.5297T>C
ENST00000681158.1:c.3179T>C
ENST00000681203.1:c.3523T>C	ENSP00000506456.1:p.Cys1175Arg
ENST00000681371.1:n.3467T>C
ENST00000681425.1:n.4073T>C
ENST00000681639.1:n.1874T>C
ENST00000328194.7:c.3595T>C	ENSP00000328524.3:p.Cys1199Arg
ENST00000525784.5:c.531T>C
ENST00000527700.5:n.3157T>C
ENST00000528725.5:c.291T>C
ENST00000529977.5:n.1496T>C
ENST00000530044.5:c.3595T>C	ENSP00000435866.1:p.Cys1199Arg
ENST00000531747.1:c.831T>C
ENST00000533737.5:c.258T>C
NM_001243254.1:c.3595T>C	NP_001230183.1:p.Cys1199Arg
NM_015213.3:c.3595T>C	NP_056028.2:p.Cys1199Arg
XM_005252832.1:c.3595T>C	XP_005252889.1:p.Cys1199Arg
XM_011519952.1:c.3595T>C	XP_011518254.1:p.Cys1199Arg
XM_011519953.1:c.1693T>C	XP_011518255.1:p.Cys565Arg
XR_242782.2:n.3777T>C
XR_930851.1:n.3777T>C
NM_001348749.1:c.3523T>C	NP_001335678.1:p.Cys1175Arg
NM_001348750.1:c.3307T>C	NP_001335679.1:p.Cys1103Arg
NR_145966.2:n.3769T>C
NM_015213.4:c.3595T>C MANE Select	NP_056028.2:p.Cys1199Arg
NM_001243254.2:c.3595T>C	NP_001230183.1:p.Cys1199Arg
NM_001348749.2:c.3523T>C	NP_001335678.1:p.Cys1175Arg
NM_001348750.2:c.3307T>C	NP_001335679.1:p.Cys1103Arg