Canonical Allele Identifier: CA5062887

Gene: EXOSC3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37785034G>A , CM000671.2:g.37785034G>A	GRCh38
NC_000009.11:g.37785031G>A , CM000671.1:g.37785031G>A	GRCh37
NC_000009.10:g.37775031G>A	NCBI36
NG_032780.1:g.5059C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_016042.4:c.11C>T MANE Select	NP_057126.2:p.Pro4Leu
ENST00000327304.10:c.11C>T MANE Select	ENSP00000323046.4:p.Pro4Leu
NM_001002269.2:c.11C>T	NP_001002269.1:p.Pro4Leu
NM_016042.3:c.11C>T	NP_057126.2:p.Pro4Leu
ENST00000327304.9:c.11C>T	ENSP00000323046.4:p.Pro4Leu
ENST00000396521.3:c.11C>T	ENSP00000379775.3:p.Pro4Leu
ENST00000465229.5:c.11C>T	ENSP00000418422.1:p.Pro4Leu
ENST00000482614.5:n.86-971C>T
ENST00000489414.5:n.44-971C>T
ENST00000540557.1:c.*761-971C>T	ENSP00000457548.1:n.*761-971C>T
ENST00000678095.1:c.-70-971C>T	ENSP00000503205.1:n.-70-971C>T
ENST00000678588.1:n.31C>T
ENST00000679059.1:c.11C>T	ENSP00000503947.1:p.Pro4Leu