Canonical Allele Identifier: CA1951492093

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204243G= , CM000673.2:g.9204243G=	GRCh38
NC_000011.9:g.9225790G= , CM000673.1:g.9225790G=	GRCh37
NC_000011.8:g.9182366G=	NCBI36
NG_053019.1:g.66093C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.366C= MANE Select	ENSP00000328524.3:p.Ile122=
ENST00000530780.2:c.*192C=	ENSP00000433925.1:n.*192C=
ENST00000530867.2:n.155C=
ENST00000532696.2:n.289C=
ENST00000679446.1:n.287C=
ENST00000679460.1:n.155C=
ENST00000679568.1:c.366C=	ENSP00000505860.1:p.Ile122=
ENST00000679745.1:n.155C=
ENST00000679999.1:c.366C=	ENSP00000505198.1:p.Ile122=
ENST00000680252.1:c.155C=
ENST00000680294.1:c.366C=	ENSP00000506113.1:p.Ile122=
ENST00000680470.1:c.366C=	ENSP00000505975.1:p.Ile122=
ENST00000680554.1:c.78C=	ENSP00000505621.1:p.Ile26=
ENST00000680576.1:n.155C=
ENST00000680599.1:n.283C=
ENST00000680742.1:c.366C=	ENSP00000505206.1:p.Ile122=
ENST00000680885.1:n.287C=
ENST00000681158.1:c.155C=
ENST00000681173.1:n.155C=
ENST00000681203.1:c.294C=	ENSP00000506456.1:p.Ile98=
ENST00000681425.1:n.287C=
ENST00000681915.1:n.155C=
ENST00000328194.7:c.366C=	ENSP00000328524.3:p.Ile122=
ENST00000526707.5:c.294C=	ENSP00000436780.1:p.Ile98=
ENST00000530044.5:c.366C=	ENSP00000435866.1:p.Ile122=
ENST00000530780.1:c.*192C=	ENSP00000433925.1:n.*192C=
ENST00000532696.1:n.121C=
NM_001243254.1:c.366C=	NP_001230183.1:p.Ile122=
NM_015213.3:c.366C=	NP_056028.2:p.Ile122=
XM_005252832.1:c.366C=	XP_005252889.1:p.Ile122=
XM_011519952.1:c.366C=	XP_011518254.1:p.Ile122=
XR_242782.2:n.631C=
XR_930851.1:n.631C=
XR_930852.1:n.631C=
XR_930853.1:n.631C=
NM_001348749.1:c.294C=	NP_001335678.1:p.Ile98=
NM_001348750.1:c.78C=	NP_001335679.1:p.Ile26=
NR_145966.2:n.623C=
NM_015213.4:c.366C= MANE Select	NP_056028.2:p.Ile122=
NM_001243254.2:c.366C=	NP_001230183.1:p.Ile122=
NM_001348749.2:c.294C=	NP_001335678.1:p.Ile98=
NM_001348750.2:c.78C=	NP_001335679.1:p.Ile26=