Canonical Allele Identifier: CA395666433

Gene: FUS

Linked Data

• gnomAD v4: 16-31183872-C-G
• COSMIC: COSM5754843 ; COSM5754844
• MyVariant Identifiers: chr16:g.31195193C>G (hg19) ; chr16:g.31183872C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183872C>G , CM000678.2:g.31183872C>G	GRCh38
NC_000016.9:g.31195193C>G , CM000678.1:g.31195193C>G	GRCh37
NC_000016.8:g.31102694C>G	NCBI36
NG_012889.2:g.8741C>G , LRG_655:g.8741C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.205C>G MANE Select	ENSP00000254108.8:p.Gln69Glu
ENST00000254108.11:c.205C>G	ENSP00000254108.7:p.Gln69Glu
ENST00000380244.7:c.202C>G	ENSP00000369594.3:p.Gln68Glu
ENST00000487509.6:n.270C>G
ENST00000487974.1:n.323C>G
ENST00000566605.5:c.205C>G	ENSP00000455073.1:p.Gln69Glu
ENST00000568685.1:c.205C>G	ENSP00000455282.1:p.Gln69Glu
NM_001170634.1:c.202C>G	NP_001164105.1:p.Gln68Glu
NM_001170937.1:c.205C>G	NP_001164408.1:p.Gln69Glu
NM_004960.3:c.205C>G , LRG_655t1:c.205C>G	NP_004951.1:p.Gln69Glu
NR_028388.2:n.310C>G
XM_005255233.3:c.-376C>G	XP_005255290.1:n.-376C>G
XM_011545781.1:c.205C>G	XP_011544083.1:p.Gln69Glu
XM_005255233.5:c.-376C>G	XP_005255290.1:n.-376C>G
XM_024450221.1:c.202C>G	XP_024305989.1:p.Gln68Glu
NM_004960.4:c.205C>G MANE Select	NP_004951.1:p.Gln69Glu