Canonical Allele Identifier: CA1951454104

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142071A= , CM000673.2:g.9142071A=	GRCh38
NC_000011.9:g.9163618A= , CM000673.1:g.9163618A=	GRCh37
NC_000011.8:g.9120194A=	NCBI36
NG_053019.1:g.128265T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3549T= MANE Select	ENSP00000328524.3:p.Asn1183=
ENST00000525784.6:n.1411T=
ENST00000530780.2:c.*3375T=	ENSP00000433925.1:n.*3375T=
ENST00000531747.2:n.3220T=
ENST00000679446.1:n.3470T=
ENST00000679458.1:n.4950T=
ENST00000679460.1:n.4611T=
ENST00000679568.1:c.3549T=	ENSP00000505860.1:p.Asn1183=
ENST00000679745.1:n.4054T=
ENST00000679773.1:n.2710T=
ENST00000679926.1:n.4851T=
ENST00000679999.1:c.*606T=	ENSP00000505198.1:n.*606T=
ENST00000680252.1:c.3216T=
ENST00000680294.1:c.3342T=	ENSP00000506113.1:p.Asn1114=
ENST00000680358.1:n.2848T=
ENST00000680470.1:c.*1330T=	ENSP00000505975.1:n.*1330T=
ENST00000680554.1:c.*82T=	ENSP00000505621.1:n.*82T=
ENST00000680576.1:n.5025T=
ENST00000680599.1:n.3590T=
ENST00000680742.1:c.*82T=	ENSP00000505206.1:n.*82T=
ENST00000680791.1:n.2433T=
ENST00000680885.1:n.5251T=
ENST00000681158.1:c.3133T=
ENST00000681203.1:c.3477T=	ENSP00000506456.1:p.Asn1159=
ENST00000681371.1:n.3421T=
ENST00000681425.1:n.4027T=
ENST00000681639.1:n.1828T=
ENST00000328194.7:c.3549T=	ENSP00000328524.3:p.Asn1183=
ENST00000525784.5:c.485T=
ENST00000527700.5:n.3111T=
ENST00000528725.5:c.245T=
ENST00000529977.5:n.1450T=
ENST00000530044.5:c.3549T=	ENSP00000435866.1:p.Asn1183=
ENST00000531747.1:c.785T=
ENST00000533737.5:c.212T=
NM_001243254.1:c.3549T=	NP_001230183.1:p.Asn1183=
NM_015213.3:c.3549T=	NP_056028.2:p.Asn1183=
XM_005252832.1:c.3549T=	XP_005252889.1:p.Asn1183=
XM_011519952.1:c.3549T=	XP_011518254.1:p.Asn1183=
XM_011519953.1:c.1647T=	XP_011518255.1:p.Asn549=
XR_242782.2:n.3731T=
XR_930851.1:n.3731T=
NM_001348749.1:c.3477T=	NP_001335678.1:p.Asn1159=
NM_001348750.1:c.3261T=	NP_001335679.1:p.Asn1087=
NR_145966.2:n.3723T=
NM_015213.4:c.3549T= MANE Select	NP_056028.2:p.Asn1183=
NM_001243254.2:c.3549T=	NP_001230183.1:p.Asn1183=
NM_001348749.2:c.3477T=	NP_001335678.1:p.Asn1159=
NM_001348750.2:c.3261T=	NP_001335679.1:p.Asn1087=