Canonical Allele Identifier: CA1951454111

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142084G= , CM000673.2:g.9142084G=	GRCh38
NC_000011.9:g.9163631G= , CM000673.1:g.9163631G=	GRCh37
NC_000011.8:g.9120207G=	NCBI36
NG_053019.1:g.128252C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3536C= MANE Select	ENSP00000328524.3:p.Thr1179=
ENST00000525784.6:n.1398C=
ENST00000530780.2:c.*3362C=	ENSP00000433925.1:n.*3362C=
ENST00000531747.2:n.3207C=
ENST00000679446.1:n.3457C=
ENST00000679458.1:n.4937C=
ENST00000679460.1:n.4598C=
ENST00000679568.1:c.3536C=	ENSP00000505860.1:p.Thr1179=
ENST00000679745.1:n.4041C=
ENST00000679773.1:n.2697C=
ENST00000679926.1:n.4838C=
ENST00000679999.1:c.*593C=	ENSP00000505198.1:n.*593C=
ENST00000680252.1:c.3203C=
ENST00000680294.1:c.3329C=	ENSP00000506113.1:p.Thr1110=
ENST00000680358.1:n.2835C=
ENST00000680470.1:c.*1317C=	ENSP00000505975.1:n.*1317C=
ENST00000680554.1:c.*69C=	ENSP00000505621.1:n.*69C=
ENST00000680576.1:n.5012C=
ENST00000680599.1:n.3577C=
ENST00000680742.1:c.*69C=	ENSP00000505206.1:n.*69C=
ENST00000680791.1:n.2420C=
ENST00000680885.1:n.5238C=
ENST00000681158.1:c.3120C=
ENST00000681203.1:c.3464C=	ENSP00000506456.1:p.Thr1155=
ENST00000681371.1:n.3408C=
ENST00000681425.1:n.4014C=
ENST00000681639.1:n.1815C=
ENST00000328194.7:c.3536C=	ENSP00000328524.3:p.Thr1179=
ENST00000525784.5:c.472C=
ENST00000527700.5:n.3098C=
ENST00000528725.5:c.232C=
ENST00000529977.5:n.1437C=
ENST00000530044.5:c.3536C=	ENSP00000435866.1:p.Thr1179=
ENST00000531747.1:c.772C=
ENST00000533737.5:c.199C=
NM_001243254.1:c.3536C=	NP_001230183.1:p.Thr1179=
NM_015213.3:c.3536C=	NP_056028.2:p.Thr1179=
XM_005252832.1:c.3536C=	XP_005252889.1:p.Thr1179=
XM_011519952.1:c.3536C=	XP_011518254.1:p.Thr1179=
XM_011519953.1:c.1634C=	XP_011518255.1:p.Thr545=
XR_242782.2:n.3718C=
XR_930851.1:n.3718C=
NM_001348749.1:c.3464C=	NP_001335678.1:p.Thr1155=
NM_001348750.1:c.3248C=	NP_001335679.1:p.Thr1083=
NR_145966.2:n.3710C=
NM_015213.4:c.3536C= MANE Select	NP_056028.2:p.Thr1179=
NM_001243254.2:c.3536C=	NP_001230183.1:p.Thr1179=
NM_001348749.2:c.3464C=	NP_001335678.1:p.Thr1155=
NM_001348750.2:c.3248C=	NP_001335679.1:p.Thr1083=