Canonical Allele Identifier: CA1951454074

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142011A= , CM000673.2:g.9142011A=	GRCh38
NC_000011.9:g.9163558A= , CM000673.1:g.9163558A=	GRCh37
NC_000011.8:g.9120134A=	NCBI36
NG_053019.1:g.128325T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3609T= MANE Select	ENSP00000328524.3:p.Thr1203=
ENST00000525784.6:n.1471T=
ENST00000530780.2:c.*3435T=	ENSP00000433925.1:n.*3435T=
ENST00000531747.2:n.3280T=
ENST00000679446.1:n.3530T=
ENST00000679458.1:n.5010T=
ENST00000679460.1:n.4671T=
ENST00000679568.1:c.3609T=	ENSP00000505860.1:p.Thr1203=
ENST00000679745.1:n.4114T=
ENST00000679773.1:n.2770T=
ENST00000679926.1:n.4911T=
ENST00000679999.1:c.*666T=	ENSP00000505198.1:n.*666T=
ENST00000680252.1:c.3276T=
ENST00000680294.1:c.3402T=	ENSP00000506113.1:p.Thr1134=
ENST00000680358.1:n.2908T=
ENST00000680470.1:c.*1390T=	ENSP00000505975.1:n.*1390T=
ENST00000680554.1:c.*142T=	ENSP00000505621.1:n.*142T=
ENST00000680576.1:n.5085T=
ENST00000680599.1:n.3650T=
ENST00000680742.1:c.*142T=	ENSP00000505206.1:n.*142T=
ENST00000680791.1:n.2493T=
ENST00000680885.1:n.5311T=
ENST00000681158.1:c.3193T=
ENST00000681203.1:c.3537T=	ENSP00000506456.1:p.Thr1179=
ENST00000681371.1:n.3481T=
ENST00000681425.1:n.4087T=
ENST00000681639.1:n.1888T=
ENST00000328194.7:c.3609T=	ENSP00000328524.3:p.Thr1203=
ENST00000525784.5:c.545T=
ENST00000527700.5:n.3171T=
ENST00000528725.5:c.305T=
ENST00000529977.5:n.1510T=
ENST00000530044.5:c.3609T=	ENSP00000435866.1:p.Thr1203=
ENST00000531747.1:c.845T=
ENST00000533737.5:c.272T=
NM_001243254.1:c.3609T=	NP_001230183.1:p.Thr1203=
NM_015213.3:c.3609T=	NP_056028.2:p.Thr1203=
XM_005252832.1:c.3609T=	XP_005252889.1:p.Thr1203=
XM_011519952.1:c.3609T=	XP_011518254.1:p.Thr1203=
XM_011519953.1:c.1707T=	XP_011518255.1:p.Thr569=
XR_242782.2:n.3791T=
XR_930851.1:n.3791T=
NM_001348749.1:c.3537T=	NP_001335678.1:p.Thr1179=
NM_001348750.1:c.3321T=	NP_001335679.1:p.Thr1107=
NR_145966.2:n.3783T=
NM_015213.4:c.3609T= MANE Select	NP_056028.2:p.Thr1203=
NM_001243254.2:c.3609T=	NP_001230183.1:p.Thr1203=
NM_001348749.2:c.3537T=	NP_001335678.1:p.Thr1179=
NM_001348750.2:c.3321T=	NP_001335679.1:p.Thr1107=