Canonical Allele Identifier: CA1951491965

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9203957C= , CM000673.2:g.9203957C=	GRCh38
NC_000011.9:g.9225504C= , CM000673.1:g.9225504C=	GRCh37
NC_000011.8:g.9182080C=	NCBI36
NG_053019.1:g.66379G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.652G= MANE Select	ENSP00000328524.3:p.Ala218=
ENST00000530780.2:c.*478G=	ENSP00000433925.1:n.*478G=
ENST00000530867.2:n.441G=
ENST00000532696.2:n.575G=
ENST00000679446.1:n.573G=
ENST00000679460.1:n.441G=
ENST00000679568.1:c.652G=	ENSP00000505860.1:p.Ala218=
ENST00000679745.1:n.441G=
ENST00000679999.1:c.652G=	ENSP00000505198.1:p.Ala218=
ENST00000680252.1:c.441G=
ENST00000680294.1:c.652G=	ENSP00000506113.1:p.Ala218=
ENST00000680470.1:c.652G=	ENSP00000505975.1:p.Ala218=
ENST00000680554.1:c.364G=	ENSP00000505621.1:p.Ala122=
ENST00000680576.1:n.441G=
ENST00000680599.1:n.569G=
ENST00000680742.1:c.652G=	ENSP00000505206.1:p.Ala218=
ENST00000680885.1:n.573G=
ENST00000681158.1:c.441G=
ENST00000681173.1:n.441G=
ENST00000681203.1:c.580G=	ENSP00000506456.1:p.Ala194=
ENST00000681425.1:n.573G=
ENST00000681915.1:n.441G=
ENST00000328194.7:c.652G=	ENSP00000328524.3:p.Ala218=
ENST00000526707.5:c.580G=	ENSP00000436780.1:p.Ala194=
ENST00000530044.5:c.652G=	ENSP00000435866.1:p.Ala218=
ENST00000532696.1:n.407G=
NM_001243254.1:c.652G=	NP_001230183.1:p.Ala218=
NM_015213.3:c.652G=	NP_056028.2:p.Ala218=
XM_005252832.1:c.652G=	XP_005252889.1:p.Ala218=
XM_011519952.1:c.652G=	XP_011518254.1:p.Ala218=
XR_242782.2:n.917G=
XR_930851.1:n.917G=
XR_930852.1:n.917G=
XR_930853.1:n.917G=
NM_001348749.1:c.580G=	NP_001335678.1:p.Ala194=
NM_001348750.1:c.364G=	NP_001335679.1:p.Ala122=
NR_145966.2:n.909G=
NM_015213.4:c.652G= MANE Select	NP_056028.2:p.Ala218=
NM_001243254.2:c.652G=	NP_001230183.1:p.Ala218=
NM_001348749.2:c.580G=	NP_001335678.1:p.Ala194=
NM_001348750.2:c.364G=	NP_001335679.1:p.Ala122=