Canonical Allele Identifier: CA1951491941

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9203902G= , CM000673.2:g.9203902G=	GRCh38
NC_000011.9:g.9225449G= , CM000673.1:g.9225449G=	GRCh37
NC_000011.8:g.9182025G=	NCBI36
NG_053019.1:g.66434C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.707C= MANE Select	ENSP00000328524.3:p.Pro236=
ENST00000530780.2:c.*533C=	ENSP00000433925.1:n.*533C=
ENST00000530867.2:n.496C=
ENST00000532696.2:n.630C=
ENST00000679446.1:n.628C=
ENST00000679460.1:n.496C=
ENST00000679568.1:c.707C=	ENSP00000505860.1:p.Pro236=
ENST00000679745.1:n.496C=
ENST00000679999.1:c.707C=	ENSP00000505198.1:p.Pro236=
ENST00000680252.1:c.496C=
ENST00000680294.1:c.707C=	ENSP00000506113.1:p.Pro236=
ENST00000680470.1:c.707C=	ENSP00000505975.1:p.Pro236=
ENST00000680554.1:c.419C=	ENSP00000505621.1:p.Pro140=
ENST00000680576.1:n.496C=
ENST00000680599.1:n.624C=
ENST00000680742.1:c.707C=	ENSP00000505206.1:p.Pro236=
ENST00000680885.1:n.628C=
ENST00000681158.1:c.496C=
ENST00000681173.1:n.496C=
ENST00000681203.1:c.635C=	ENSP00000506456.1:p.Pro212=
ENST00000681425.1:n.628C=
ENST00000681915.1:n.496C=
ENST00000328194.7:c.707C=	ENSP00000328524.3:p.Pro236=
ENST00000526707.5:c.635C=	ENSP00000436780.1:p.Pro212=
ENST00000530044.5:c.707C=	ENSP00000435866.1:p.Pro236=
ENST00000532696.1:n.462C=
NM_001243254.1:c.707C=	NP_001230183.1:p.Pro236=
NM_015213.3:c.707C=	NP_056028.2:p.Pro236=
XM_005252832.1:c.707C=	XP_005252889.1:p.Pro236=
XM_011519952.1:c.707C=	XP_011518254.1:p.Pro236=
XR_242782.2:n.972C=
XR_930851.1:n.972C=
XR_930852.1:n.972C=
XR_930853.1:n.972C=
NM_001348749.1:c.635C=	NP_001335678.1:p.Pro212=
NM_001348750.1:c.419C=	NP_001335679.1:p.Pro140=
NR_145966.2:n.964C=
NM_015213.4:c.707C= MANE Select	NP_056028.2:p.Pro236=
NM_001243254.2:c.707C=	NP_001230183.1:p.Pro236=
NM_001348749.2:c.635C=	NP_001335678.1:p.Pro212=
NM_001348750.2:c.419C=	NP_001335679.1:p.Pro140=