Canonical Allele Identifier: CA1951492002

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204030G= , CM000673.2:g.9204030G=	GRCh38
NC_000011.9:g.9225577G= , CM000673.1:g.9225577G=	GRCh37
NC_000011.8:g.9182153G=	NCBI36
NG_053019.1:g.66306C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.579C= MANE Select	ENSP00000328524.3:p.Ser193=
ENST00000530780.2:c.*405C=	ENSP00000433925.1:n.*405C=
ENST00000530867.2:n.368C=
ENST00000532696.2:n.502C=
ENST00000679446.1:n.500C=
ENST00000679460.1:n.368C=
ENST00000679568.1:c.579C=	ENSP00000505860.1:p.Ser193=
ENST00000679745.1:n.368C=
ENST00000679999.1:c.579C=	ENSP00000505198.1:p.Ser193=
ENST00000680252.1:c.368C=
ENST00000680294.1:c.579C=	ENSP00000506113.1:p.Ser193=
ENST00000680470.1:c.579C=	ENSP00000505975.1:p.Ser193=
ENST00000680554.1:c.291C=	ENSP00000505621.1:p.Ser97=
ENST00000680576.1:n.368C=
ENST00000680599.1:n.496C=
ENST00000680742.1:c.579C=	ENSP00000505206.1:p.Ser193=
ENST00000680885.1:n.500C=
ENST00000681158.1:c.368C=
ENST00000681173.1:n.368C=
ENST00000681203.1:c.507C=	ENSP00000506456.1:p.Ser169=
ENST00000681425.1:n.500C=
ENST00000681915.1:n.368C=
ENST00000328194.7:c.579C=	ENSP00000328524.3:p.Ser193=
ENST00000526707.5:c.507C=	ENSP00000436780.1:p.Ser169=
ENST00000530044.5:c.579C=	ENSP00000435866.1:p.Ser193=
ENST00000532696.1:n.334C=
NM_001243254.1:c.579C=	NP_001230183.1:p.Ser193=
NM_015213.3:c.579C=	NP_056028.2:p.Ser193=
XM_005252832.1:c.579C=	XP_005252889.1:p.Ser193=
XM_011519952.1:c.579C=	XP_011518254.1:p.Ser193=
XR_242782.2:n.844C=
XR_930851.1:n.844C=
XR_930852.1:n.844C=
XR_930853.1:n.844C=
NM_001348749.1:c.507C=	NP_001335678.1:p.Ser169=
NM_001348750.1:c.291C=	NP_001335679.1:p.Ser97=
NR_145966.2:n.836C=
NM_015213.4:c.579C= MANE Select	NP_056028.2:p.Ser193=
NM_001243254.2:c.579C=	NP_001230183.1:p.Ser193=
NM_001348749.2:c.507C=	NP_001335678.1:p.Ser169=
NM_001348750.2:c.291C=	NP_001335679.1:p.Ser97=