Canonical Allele Identifier: CA395672436

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200526C>G (hg19) ; chr16:g.31189205C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189205C>G , CM000678.2:g.31189205C>G	GRCh38
NC_000016.9:g.31200526C>G , CM000678.1:g.31200526C>G	GRCh37
NC_000016.8:g.31108027C>G	NCBI36
NG_012889.2:g.14074C>G , LRG_655:g.14074C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.915C>G MANE Select	ENSP00000254108.8:p.Phe305Leu
ENST00000254108.11:c.915C>G	ENSP00000254108.7:p.Phe305Leu
ENST00000380244.7:c.912C>G	ENSP00000369594.3:p.Phe304Leu
ENST00000474990.5:n.209C>G
ENST00000487509.6:n.4090C>G
ENST00000564766.1:n.739C>G
ENST00000566605.5:c.*88C>G	ENSP00000455073.1:n.*88C>G
ENST00000568685.1:c.918C>G	ENSP00000455282.1:p.Phe306Leu
ENST00000568901.2:n.289C>G
NM_001170634.1:c.912C>G	NP_001164105.1:p.Phe304Leu
NM_001170937.1:c.903C>G	NP_001164408.1:p.Phe301Leu
NM_004960.3:c.915C>G , LRG_655t1:c.915C>G	NP_004951.1:p.Phe305Leu
NR_028388.2:n.985C>G
XM_005255233.3:c.300C>G	XP_005255290.1:p.Phe100Leu
XM_011545781.1:c.909C>G	XP_011544083.1:p.Phe303Leu
XM_011545782.1:c.300C>G	XP_011544084.1:p.Phe100Leu
XM_005255233.5:c.300C>G	XP_005255290.1:p.Phe100Leu
XM_011545782.2:c.300C>G	XP_011544084.1:p.Phe100Leu
XM_024450221.1:c.906C>G	XP_024305989.1:p.Phe302Leu
NM_004960.4:c.915C>G MANE Select	NP_004951.1:p.Phe305Leu