Canonical Allele Identifier: CA395669534

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196271C>T (hg19) ; chr16:g.31184950C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184950C>T , CM000678.2:g.31184950C>T	GRCh38
NC_000016.9:g.31196271C>T , CM000678.1:g.31196271C>T	GRCh37
NC_000016.8:g.31103772C>T	NCBI36
NG_012889.2:g.9819C>T , LRG_655:g.9819C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.535C>T MANE Select	ENSP00000254108.8:p.Gln179Ter
ENST00000254108.11:c.535C>T	ENSP00000254108.7:p.Gln179Ter
ENST00000380244.7:c.532C>T	ENSP00000369594.3:p.Gln178Ter
ENST00000487509.6:n.600C>T
ENST00000566605.5:c.535C>T	ENSP00000455073.1:p.Gln179Ter
ENST00000568685.1:c.535C>T	ENSP00000455282.1:p.Gln179Ter
NM_001170634.1:c.532C>T	NP_001164105.1:p.Gln178Ter
NM_001170937.1:c.523C>T	NP_001164408.1:p.Gln175Ter
NM_004960.3:c.535C>T , LRG_655t1:c.535C>T	NP_004951.1:p.Gln179Ter
NR_028388.2:n.640C>T
XM_005255233.3:c.-46C>T	XP_005255290.1:n.-46C>T
XM_011545781.1:c.529C>T	XP_011544083.1:p.Gln177Ter
XM_011545782.1:c.-46C>T	XP_011544084.1:n.-46C>T
XM_005255233.5:c.-46C>T	XP_005255290.1:n.-46C>T
XM_011545782.2:c.-46C>T	XP_011544084.1:n.-46C>T
XM_024450221.1:c.526C>T	XP_024305989.1:p.Gln176Ter
NM_004960.4:c.535C>T MANE Select	NP_004951.1:p.Gln179Ter