Canonical Allele Identifier: CA1951454065

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141987G= , CM000673.2:g.9141987G=	GRCh38
NC_000011.9:g.9163534G= , CM000673.1:g.9163534G=	GRCh37
NC_000011.8:g.9120110G=	NCBI36
NG_053019.1:g.128349C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3633C= MANE Select	ENSP00000328524.3:p.Asn1211=
ENST00000525784.6:n.1495C=
ENST00000530780.2:c.*3459C=	ENSP00000433925.1:n.*3459C=
ENST00000531747.2:n.3304C=
ENST00000679446.1:n.3554C=
ENST00000679458.1:n.5034C=
ENST00000679460.1:n.4695C=
ENST00000679568.1:c.3633C=	ENSP00000505860.1:p.Asn1211=
ENST00000679745.1:n.4138C=
ENST00000679773.1:n.2794C=
ENST00000679926.1:n.4935C=
ENST00000679999.1:c.*690C=	ENSP00000505198.1:n.*690C=
ENST00000680252.1:c.3300C=
ENST00000680294.1:c.3426C=	ENSP00000506113.1:p.Asn1142=
ENST00000680358.1:n.2932C=
ENST00000680470.1:c.*1414C=	ENSP00000505975.1:n.*1414C=
ENST00000680554.1:c.*166C=	ENSP00000505621.1:n.*166C=
ENST00000680576.1:n.5109C=
ENST00000680599.1:n.3674C=
ENST00000680742.1:c.*166C=	ENSP00000505206.1:n.*166C=
ENST00000680791.1:n.2517C=
ENST00000680885.1:n.5335C=
ENST00000681158.1:c.3217C=
ENST00000681203.1:c.3561C=	ENSP00000506456.1:p.Asn1187=
ENST00000681371.1:n.3505C=
ENST00000681425.1:n.4111C=
ENST00000681639.1:n.1912C=
ENST00000328194.7:c.3633C=	ENSP00000328524.3:p.Asn1211=
ENST00000525784.5:c.569C=
ENST00000527700.5:n.3195C=
ENST00000528725.5:c.329C=
ENST00000529977.5:n.1534C=
ENST00000530044.5:c.3633C=	ENSP00000435866.1:p.Asn1211=
ENST00000531747.1:c.869C=
ENST00000533737.5:c.296C=
NM_001243254.1:c.3633C=	NP_001230183.1:p.Asn1211=
NM_015213.3:c.3633C=	NP_056028.2:p.Asn1211=
XM_005252832.1:c.3633C=	XP_005252889.1:p.Asn1211=
XM_011519952.1:c.3633C=	XP_011518254.1:p.Asn1211=
XM_011519953.1:c.1731C=	XP_011518255.1:p.Asn577=
XR_242782.2:n.3815C=
XR_930851.1:n.3815C=
NM_001348749.1:c.3561C=	NP_001335678.1:p.Asn1187=
NM_001348750.1:c.3345C=	NP_001335679.1:p.Asn1115=
NR_145966.2:n.3807C=
NM_015213.4:c.3633C= MANE Select	NP_056028.2:p.Asn1211=
NM_001243254.2:c.3633C=	NP_001230183.1:p.Asn1211=
NM_001348749.2:c.3561C=	NP_001335678.1:p.Asn1187=
NM_001348750.2:c.3345C=	NP_001335679.1:p.Asn1115=