Canonical Allele Identifier: CA373476102

Gene: EXOSC3

Linked Data

• gnomAD v4: 9-37784969-G-A
• MyVariant Identifiers: chr9:g.37784966G>A (hg19) ; chr9:g.37784969G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.37784969G>A , CM000671.2:g.37784969G>A	GRCh38
NC_000009.11:g.37784966G>A , CM000671.1:g.37784966G>A	GRCh37
NC_000009.10:g.37774966G>A	NCBI36
NG_032780.1:g.5124C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000327304.10:c.76C>T MANE Select	ENSP00000323046.4:p.Gln26Ter
ENST00000678095.1:c.-70-906C>T	ENSP00000503205.1:n.-70-906C>T
ENST00000678588.1:n.96C>T
ENST00000679059.1:c.76C>T	ENSP00000503947.1:p.Gln26Ter
ENST00000327304.9:c.76C>T	ENSP00000323046.4:p.Gln26Ter
ENST00000396521.3:c.76C>T	ENSP00000379775.3:p.Gln26Ter
ENST00000465229.5:c.76C>T	ENSP00000418422.1:p.Gln26Ter
ENST00000482614.5:n.86-906C>T
ENST00000489414.5:n.44-906C>T
ENST00000540557.1:c.*761-906C>T	ENSP00000457548.1:n.*761-906C>T
NM_001002269.2:c.76C>T	NP_001002269.1:p.Gln26Ter
NM_016042.3:c.76C>T	NP_057126.2:p.Gln26Ter
NM_016042.4:c.76C>T MANE Select	NP_057126.2:p.Gln26Ter