Canonical Allele Identifier: CA1951454097

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142061G= , CM000673.2:g.9142061G=	GRCh38
NC_000011.9:g.9163608G= , CM000673.1:g.9163608G=	GRCh37
NC_000011.8:g.9120184G=	NCBI36
NG_053019.1:g.128275C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3559C= MANE Select	ENSP00000328524.3:p.Pro1187=
ENST00000525784.6:n.1421C=
ENST00000530780.2:c.*3385C=	ENSP00000433925.1:n.*3385C=
ENST00000531747.2:n.3230C=
ENST00000679446.1:n.3480C=
ENST00000679458.1:n.4960C=
ENST00000679460.1:n.4621C=
ENST00000679568.1:c.3559C=	ENSP00000505860.1:p.Pro1187=
ENST00000679745.1:n.4064C=
ENST00000679773.1:n.2720C=
ENST00000679926.1:n.4861C=
ENST00000679999.1:c.*616C=	ENSP00000505198.1:n.*616C=
ENST00000680252.1:c.3226C=
ENST00000680294.1:c.3352C=	ENSP00000506113.1:p.Pro1118=
ENST00000680358.1:n.2858C=
ENST00000680470.1:c.*1340C=	ENSP00000505975.1:n.*1340C=
ENST00000680554.1:c.*92C=	ENSP00000505621.1:n.*92C=
ENST00000680576.1:n.5035C=
ENST00000680599.1:n.3600C=
ENST00000680742.1:c.*92C=	ENSP00000505206.1:n.*92C=
ENST00000680791.1:n.2443C=
ENST00000680885.1:n.5261C=
ENST00000681158.1:c.3143C=
ENST00000681203.1:c.3487C=	ENSP00000506456.1:p.Pro1163=
ENST00000681371.1:n.3431C=
ENST00000681425.1:n.4037C=
ENST00000681639.1:n.1838C=
ENST00000328194.7:c.3559C=	ENSP00000328524.3:p.Pro1187=
ENST00000525784.5:c.495C=
ENST00000527700.5:n.3121C=
ENST00000528725.5:c.255C=
ENST00000529977.5:n.1460C=
ENST00000530044.5:c.3559C=	ENSP00000435866.1:p.Pro1187=
ENST00000531747.1:c.795C=
ENST00000533737.5:c.222C=
NM_001243254.1:c.3559C=	NP_001230183.1:p.Pro1187=
NM_015213.3:c.3559C=	NP_056028.2:p.Pro1187=
XM_005252832.1:c.3559C=	XP_005252889.1:p.Pro1187=
XM_011519952.1:c.3559C=	XP_011518254.1:p.Pro1187=
XM_011519953.1:c.1657C=	XP_011518255.1:p.Pro553=
XR_242782.2:n.3741C=
XR_930851.1:n.3741C=
NM_001348749.1:c.3487C=	NP_001335678.1:p.Pro1163=
NM_001348750.1:c.3271C=	NP_001335679.1:p.Pro1091=
NR_145966.2:n.3733C=
NM_015213.4:c.3559C= MANE Select	NP_056028.2:p.Pro1187=
NM_001243254.2:c.3559C=	NP_001230183.1:p.Pro1187=
NM_001348749.2:c.3487C=	NP_001335678.1:p.Pro1163=
NM_001348750.2:c.3271C=	NP_001335679.1:p.Pro1091=