Canonical Allele Identifier: CA1951464508

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160834C= , CM000673.2:g.9160834C=	GRCh38
NC_000011.9:g.9182381C= , CM000673.1:g.9182381C=	GRCh37
NC_000011.8:g.9138957C=	NCBI36
NG_053019.1:g.109502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2315G= MANE Select	ENSP00000328524.3:p.Arg772=
ENST00000530780.2:c.*2141G=	ENSP00000433925.1:n.*2141G=
ENST00000679446.1:n.2236G=
ENST00000679458.1:n.3716G=
ENST00000679460.1:n.2104G=
ENST00000679568.1:c.2315G=	ENSP00000505860.1:p.Arg772=
ENST00000679745.1:n.2104G=
ENST00000679926.1:n.1131G=
ENST00000679999.1:c.2315G=	ENSP00000505198.1:p.Arg772=
ENST00000680252.1:c.2104G=
ENST00000680294.1:c.2315G=	ENSP00000506113.1:p.Arg772=
ENST00000680358.1:n.1614G=
ENST00000680470.1:c.*181G=	ENSP00000505975.1:n.*181G=
ENST00000680554.1:c.2027G=	ENSP00000505621.1:p.Arg676=
ENST00000680576.1:n.2104G=
ENST00000680599.1:n.2232G=
ENST00000680742.1:c.2315G=	ENSP00000505206.1:p.Arg772=
ENST00000680885.1:n.2236G=
ENST00000681158.1:c.2104G=
ENST00000681173.1:n.2104G=
ENST00000681203.1:c.2243G=	ENSP00000506456.1:p.Arg748=
ENST00000681425.1:n.2236G=
ENST00000328194.7:c.2315G=	ENSP00000328524.3:p.Arg772=
ENST00000526707.5:c.2243G=	ENSP00000436780.1:p.Arg748=
ENST00000527700.5:n.1877G=
ENST00000530044.5:c.2315G=	ENSP00000435866.1:p.Arg772=
NM_001243254.1:c.2315G=	NP_001230183.1:p.Arg772=
NM_015213.3:c.2315G=	NP_056028.2:p.Arg772=
XM_005252832.1:c.2315G=	XP_005252889.1:p.Arg772=
XM_011519952.1:c.2315G=	XP_011518254.1:p.Arg772=
XM_011519953.1:c.413G=	XP_011518255.1:p.Arg138=
XR_242782.2:n.2580G=
XR_930851.1:n.2580G=
XR_930852.1:n.2580G=
XR_930853.1:n.2429G=
NM_001348749.1:c.2243G=	NP_001335678.1:p.Arg748=
NM_001348750.1:c.2027G=	NP_001335679.1:p.Arg676=
NR_145966.2:n.2572G=
NM_015213.4:c.2315G= MANE Select	NP_056028.2:p.Arg772=
NM_001243254.2:c.2315G=	NP_001230183.1:p.Arg772=
NM_001348749.2:c.2243G=	NP_001335678.1:p.Arg748=
NM_001348750.2:c.2027G=	NP_001335679.1:p.Arg676=