Canonical Allele Identifier: CA217547994

Gene: DENND5A

Linked Data

• dbSNP Id: rs938418383
• gnomAD v2: 11-9225842-G-A
• gnomAD v4: 11-9204295-G-A
• COSMIC: COSM1135268
• MyVariant Identifiers: chr11:g.9225842G>A (hg19) ; chr11:g.9204295G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204295G>A , CM000673.2:g.9204295G>A	GRCh38
NC_000011.9:g.9225842G>A , CM000673.1:g.9225842G>A	GRCh37
NC_000011.8:g.9182418G>A	NCBI36
NG_053019.1:g.66041C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.314C>T MANE Select	ENSP00000328524.3:p.Ala105Val
ENST00000530780.2:c.*140C>T	ENSP00000433925.1:n.*140C>T
ENST00000530867.2:n.103C>T
ENST00000532696.2:n.237C>T
ENST00000679446.1:n.235C>T
ENST00000679460.1:n.103C>T
ENST00000679568.1:c.314C>T	ENSP00000505860.1:p.Ala105Val
ENST00000679745.1:n.103C>T
ENST00000679999.1:c.314C>T	ENSP00000505198.1:p.Ala105Val
ENST00000680252.1:c.103C>T
ENST00000680294.1:c.314C>T	ENSP00000506113.1:p.Ala105Val
ENST00000680470.1:c.314C>T	ENSP00000505975.1:p.Ala105Val
ENST00000680554.1:c.26C>T	ENSP00000505621.1:p.Ala9Val
ENST00000680576.1:n.103C>T
ENST00000680599.1:n.231C>T
ENST00000680742.1:c.314C>T	ENSP00000505206.1:p.Ala105Val
ENST00000680885.1:n.235C>T
ENST00000681158.1:c.103C>T
ENST00000681173.1:n.103C>T
ENST00000681203.1:c.242C>T	ENSP00000506456.1:p.Ala81Val
ENST00000681425.1:n.235C>T
ENST00000681915.1:n.103C>T
ENST00000328194.7:c.314C>T	ENSP00000328524.3:p.Ala105Val
ENST00000526707.5:c.242C>T	ENSP00000436780.1:p.Ala81Val
ENST00000530044.5:c.314C>T	ENSP00000435866.1:p.Ala105Val
ENST00000530780.1:c.*140C>T	ENSP00000433925.1:n.*140C>T
ENST00000532696.1:n.69C>T
NM_001243254.1:c.314C>T	NP_001230183.1:p.Ala105Val
NM_015213.3:c.314C>T	NP_056028.2:p.Ala105Val
XM_005252832.1:c.314C>T	XP_005252889.1:p.Ala105Val
XM_011519952.1:c.314C>T	XP_011518254.1:p.Ala105Val
XR_242782.2:n.579C>T
XR_930851.1:n.579C>T
XR_930852.1:n.579C>T
XR_930853.1:n.579C>T
NM_001348749.1:c.242C>T	NP_001335678.1:p.Ala81Val
NM_001348750.1:c.26C>T	NP_001335679.1:p.Ala9Val
NR_145966.2:n.571C>T
NM_015213.4:c.314C>T MANE Select	NP_056028.2:p.Ala105Val
NM_001243254.2:c.314C>T	NP_001230183.1:p.Ala105Val
NM_001348749.2:c.242C>T	NP_001335678.1:p.Ala81Val
NM_001348750.2:c.26C>T	NP_001335679.1:p.Ala9Val