Canonical Allele Identifier: CA494713655

Gene: FUS

Linked Data

• dbSNP Id: rs1309427963
• gnomAD v4: 16-31189164-C-T
• MyVariant Identifiers: chr16:g.31200485C>T (hg19) ; chr16:g.31189164C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189164C>T , CM000678.2:g.31189164C>T	GRCh38
NC_000016.9:g.31200485C>T , CM000678.1:g.31200485C>T	GRCh37
NC_000016.8:g.31107986C>T	NCBI36
NG_012889.2:g.14033C>T , LRG_655:g.14033C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.874C>T MANE Select	ENSP00000254108.8:p.Leu292=
ENST00000254108.11:c.874C>T	ENSP00000254108.7:p.Leu292=
ENST00000380244.7:c.871C>T	ENSP00000369594.3:p.Leu291=
ENST00000474990.5:n.168C>T
ENST00000487509.6:n.4049C>T
ENST00000564766.1:n.698C>T
ENST00000566605.5:c.*47C>T	ENSP00000455073.1:n.*47C>T
ENST00000568685.1:c.877C>T	ENSP00000455282.1:p.Leu293=
ENST00000568901.2:n.248C>T
NM_001170634.1:c.871C>T	NP_001164105.1:p.Leu291=
NM_001170937.1:c.862C>T	NP_001164408.1:p.Leu288=
NM_004960.3:c.874C>T , LRG_655t1:c.874C>T	NP_004951.1:p.Leu292=
NR_028388.2:n.944C>T
XM_005255233.3:c.259C>T	XP_005255290.1:p.Leu87=
XM_011545781.1:c.868C>T	XP_011544083.1:p.Leu290=
XM_011545782.1:c.259C>T	XP_011544084.1:p.Leu87=
XM_005255233.5:c.259C>T	XP_005255290.1:p.Leu87=
XM_011545782.2:c.259C>T	XP_011544084.1:p.Leu87=
XM_024450221.1:c.865C>T	XP_024305989.1:p.Leu289=
NM_004960.4:c.874C>T MANE Select	NP_004951.1:p.Leu292=