Canonical Allele Identifier: CA793396

Gene: EXO5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40515558G>A , CM000663.2:g.40515558G>A	GRCh38
NC_000001.10:g.40981230G>A , CM000663.1:g.40981230G>A	GRCh37
NC_000001.9:g.40753817G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296380.9:c.1014G>A	ENSP00000296380.4:p.Glu338=
ENST00000415550.6:c.1014G>A MANE Select	ENSP00000413565.2:p.Glu338=
ENST00000418186.2:c.1014G>A	ENSP00000391240.2:p.Glu338=
ENST00000419161.2:c.1014G>A	ENSP00000392115.2:p.Glu338=
ENST00000420209.2:c.1014G>A	ENSP00000398437.2:p.Glu338=
ENST00000432259.6:c.1014G>A	ENSP00000416857.2:p.Glu338=
ENST00000443729.6:c.1014G>A	ENSP00000409715.2:p.Glu338=
ENST00000682383.1:c.1014G>A	ENSP00000508270.1:p.Glu338=
ENST00000296380.8:c.1014G>A	ENSP00000296380.4:p.Glu338=
ENST00000358527.6:c.1014G>A	ENSP00000351328.2:p.Glu338=
ENST00000372703.1:c.1014G>A	ENSP00000361788.1:p.Glu338=
NM_022774.1:c.1014G>A	NP_073611.1:p.Glu338=
XM_005271125.2:c.1014G>A	XP_005271182.1:p.Glu338=
XM_005271126.2:c.1014G>A	XP_005271183.1:p.Glu338=
XM_005271128.2:c.1014G>A	XP_005271185.1:p.Glu338=
XM_011541970.1:c.1014G>A	XP_011540272.1:p.Glu338=
NM_001346946.1:c.1014G>A	NP_001333875.1:p.Glu338=
NM_001346947.1:c.1014G>A	NP_001333876.1:p.Glu338=
NM_001346948.1:c.1014G>A	NP_001333877.1:p.Glu338=
NM_001346949.1:c.1014G>A	NP_001333878.1:p.Glu338=
NM_001346950.1:c.1014G>A	NP_001333879.1:p.Glu338=
NM_001346951.1:c.1014G>A	NP_001333880.1:p.Glu338=
NM_001346952.1:c.1014G>A	NP_001333881.1:p.Glu338=
NM_001346953.1:c.1014G>A	NP_001333882.1:p.Glu338=
NM_001346954.1:c.1014G>A	NP_001333883.1:p.Glu338=
NM_001346955.1:c.1014G>A	NP_001333884.1:p.Glu338=
NM_001346956.1:c.1014G>A	NP_001333885.1:p.Glu338=
NM_022774.2:c.1014G>A	NP_073611.1:p.Glu338=
XM_017002099.2:c.1014G>A	XP_016857588.1:p.Glu338=
XM_017002102.2:c.1014G>A	XP_016857591.1:p.Glu338=
NM_001346946.2:c.1014G>A	NP_001333875.1:p.Glu338=
NM_001346947.2:c.1014G>A	NP_001333876.1:p.Glu338=
NM_001346948.2:c.1014G>A	NP_001333877.1:p.Glu338=
NM_001346949.2:c.1014G>A	NP_001333878.1:p.Glu338=
NM_001346950.2:c.1014G>A	NP_001333879.1:p.Glu338=
NM_001346951.2:c.1014G>A	NP_001333880.1:p.Glu338=
NM_001346952.2:c.1014G>A	NP_001333881.1:p.Glu338=
NM_001346953.2:c.1014G>A MANE Select	NP_001333882.1:p.Glu338=
NM_001346954.2:c.1014G>A	NP_001333883.1:p.Glu338=
NM_001346955.2:c.1014G>A	NP_001333884.1:p.Glu338=
NM_001346956.2:c.1014G>A	NP_001333885.1:p.Glu338=
NM_022774.3:c.1014G>A	NP_073611.1:p.Glu338=