Canonical Allele Identifier: CA395666435

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31195193C>A (hg19) ; chr16:g.31183872C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.205C>A MANE Select	ENSP00000254108.8:p.Gln69Lys
ENST00000254108.11:c.205C>A	ENSP00000254108.7:p.Gln69Lys
ENST00000380244.7:c.202C>A	ENSP00000369594.3:p.Gln68Lys
ENST00000487509.6:n.270C>A
ENST00000487974.1:n.323C>A
ENST00000566605.5:c.205C>A	ENSP00000455073.1:p.Gln69Lys
ENST00000568685.1:c.205C>A	ENSP00000455282.1:p.Gln69Lys
NM_001170634.1:c.202C>A	NP_001164105.1:p.Gln68Lys
NM_001170937.1:c.205C>A	NP_001164408.1:p.Gln69Lys
NM_004960.3:c.205C>A , LRG_655t1:c.205C>A	NP_004951.1:p.Gln69Lys
NR_028388.2:n.310C>A
XM_005255233.3:c.-376C>A	XP_005255290.1:n.-376C>A
XM_011545781.1:c.205C>A	XP_011544083.1:p.Gln69Lys
XM_005255233.5:c.-376C>A	XP_005255290.1:n.-376C>A
XM_024450221.1:c.202C>A	XP_024305989.1:p.Gln68Lys
NM_004960.4:c.205C>A MANE Select	NP_004951.1:p.Gln69Lys