Canonical Allele Identifier: CA373476041
Gene: EXOSC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.37784938A>T , CM000671.2:g.37784938A>T GRCh38
NC_000009.11:g.37784935A>T , CM000671.1:g.37784935A>T GRCh37
NC_000009.10:g.37774935A>T NCBI36
NG_032780.1:g.5155T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327304.10:c.107T>A MANE Select ENSP00000323046.4:p.Leu36Gln
ENST00000678095.1:c.-70-875T>A ENSP00000503205.1:n.-70-875T>A
ENST00000678588.1:n.127T>A
ENST00000679059.1:c.107T>A ENSP00000503947.1:p.Leu36Gln
ENST00000327304.9:c.107T>A ENSP00000323046.4:p.Leu36Gln
ENST00000396521.3:c.107T>A ENSP00000379775.3:p.Leu36Gln
ENST00000465229.5:c.107T>A ENSP00000418422.1:p.Leu36Gln
ENST00000482614.5:n.86-875T>A
ENST00000489414.5:n.44-875T>A
ENST00000540557.1:c.*761-875T>A ENSP00000457548.1:n.*761-875T>A
NM_001002269.2:c.107T>A NP_001002269.1:p.Leu36Gln
NM_016042.3:c.107T>A NP_057126.2:p.Leu36Gln
NM_016042.4:c.107T>A MANE Select NP_057126.2:p.Leu36Gln