Canonical Allele Identifier: CA395672298

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200505T>G (hg19) ; chr16:g.31189184T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189184T>G , CM000678.2:g.31189184T>G	GRCh38
NC_000016.9:g.31200505T>G , CM000678.1:g.31200505T>G	GRCh37
NC_000016.8:g.31108006T>G	NCBI36
NG_012889.2:g.14053T>G , LRG_655:g.14053T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.894T>G MANE Select	ENSP00000254108.8:p.Ile298Met
ENST00000254108.11:c.894T>G	ENSP00000254108.7:p.Ile298Met
ENST00000380244.7:c.891T>G	ENSP00000369594.3:p.Ile297Met
ENST00000474990.5:n.188T>G
ENST00000487509.6:n.4069T>G
ENST00000564766.1:n.718T>G
ENST00000566605.5:c.*67T>G	ENSP00000455073.1:n.*67T>G
ENST00000568685.1:c.897T>G	ENSP00000455282.1:p.Ile299Met
ENST00000568901.2:n.268T>G
NM_001170634.1:c.891T>G	NP_001164105.1:p.Ile297Met
NM_001170937.1:c.882T>G	NP_001164408.1:p.Ile294Met
NM_004960.3:c.894T>G , LRG_655t1:c.894T>G	NP_004951.1:p.Ile298Met
NR_028388.2:n.964T>G
XM_005255233.3:c.279T>G	XP_005255290.1:p.Ile93Met
XM_011545781.1:c.888T>G	XP_011544083.1:p.Ile296Met
XM_011545782.1:c.279T>G	XP_011544084.1:p.Ile93Met
XM_005255233.5:c.279T>G	XP_005255290.1:p.Ile93Met
XM_011545782.2:c.279T>G	XP_011544084.1:p.Ile93Met
XM_024450221.1:c.885T>G	XP_024305989.1:p.Ile295Met
NM_004960.4:c.894T>G MANE Select	NP_004951.1:p.Ile298Met