Canonical Allele Identifier: CA494710757

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31195282T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183961T>A , CM000678.2:g.31183961T>A	GRCh38
NC_000016.9:g.31195282T>A , CM000678.1:g.31195282T>A	GRCh37
NC_000016.8:g.31102783T>A	NCBI36
NG_012889.2:g.8830T>A , LRG_655:g.8830T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.294T>A MANE Select	ENSP00000254108.8:p.Pro98=
ENST00000254108.11:c.294T>A	ENSP00000254108.7:p.Pro98=
ENST00000380244.7:c.291T>A	ENSP00000369594.3:p.Pro97=
ENST00000487509.6:n.359T>A
ENST00000487974.1:n.412T>A
ENST00000566605.5:c.294T>A	ENSP00000455073.1:p.Pro98=
ENST00000568685.1:c.294T>A	ENSP00000455282.1:p.Pro98=
NM_001170634.1:c.291T>A	NP_001164105.1:p.Pro97=
NM_001170937.1:c.294T>A	NP_001164408.1:p.Pro98=
NM_004960.3:c.294T>A , LRG_655t1:c.294T>A	NP_004951.1:p.Pro98=
NR_028388.2:n.399T>A
XM_005255233.3:c.-287T>A	XP_005255290.1:n.-287T>A
XM_011545781.1:c.294T>A	XP_011544083.1:p.Pro98=
XM_005255233.5:c.-287T>A	XP_005255290.1:n.-287T>A
XM_024450221.1:c.291T>A	XP_024305989.1:p.Pro97=
NM_004960.4:c.294T>A MANE Select	NP_004951.1:p.Pro98=