Canonical Allele Identifier: CA395672526

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200542A>G (hg19) ; chr16:g.31189221A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189221A>G , CM000678.2:g.31189221A>G	GRCh38
NC_000016.9:g.31200542A>G , CM000678.1:g.31200542A>G	GRCh37
NC_000016.8:g.31108043A>G	NCBI36
NG_012889.2:g.14090A>G , LRG_655:g.14090A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.931A>G MANE Select	ENSP00000254108.8:p.Ile311Val
ENST00000254108.11:c.931A>G	ENSP00000254108.7:p.Ile311Val
ENST00000380244.7:c.928A>G	ENSP00000369594.3:p.Ile310Val
ENST00000474990.5:n.225A>G
ENST00000487509.6:n.4106A>G
ENST00000564766.1:n.755A>G
ENST00000566605.5:c.*104A>G	ENSP00000455073.1:n.*104A>G
ENST00000568685.1:c.934A>G	ENSP00000455282.1:p.Ile312Val
ENST00000568901.2:n.305A>G
NM_001170634.1:c.928A>G	NP_001164105.1:p.Ile310Val
NM_001170937.1:c.919A>G	NP_001164408.1:p.Ile307Val
NM_004960.3:c.931A>G , LRG_655t1:c.931A>G	NP_004951.1:p.Ile311Val
NR_028388.2:n.1001A>G
XM_005255233.3:c.316A>G	XP_005255290.1:p.Ile106Val
XM_011545781.1:c.925A>G	XP_011544083.1:p.Ile309Val
XM_011545782.1:c.316A>G	XP_011544084.1:p.Ile106Val
XM_005255233.5:c.316A>G	XP_005255290.1:p.Ile106Val
XM_011545782.2:c.316A>G	XP_011544084.1:p.Ile106Val
XM_024450221.1:c.922A>G	XP_024305989.1:p.Ile308Val
NM_004960.4:c.931A>G MANE Select	NP_004951.1:p.Ile311Val