Canonical Allele Identifier: CA494713695

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200511T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189190T>A , CM000678.2:g.31189190T>A	GRCh38
NC_000016.9:g.31200511T>A , CM000678.1:g.31200511T>A	GRCh37
NC_000016.8:g.31108012T>A	NCBI36
NG_012889.2:g.14059T>A , LRG_655:g.14059T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.900T>A MANE Select	ENSP00000254108.8:p.Ser300=
ENST00000254108.11:c.900T>A	ENSP00000254108.7:p.Ser300=
ENST00000380244.7:c.897T>A	ENSP00000369594.3:p.Ser299=
ENST00000474990.5:n.194T>A
ENST00000487509.6:n.4075T>A
ENST00000564766.1:n.724T>A
ENST00000566605.5:c.*73T>A	ENSP00000455073.1:n.*73T>A
ENST00000568685.1:c.903T>A	ENSP00000455282.1:p.Ser301=
ENST00000568901.2:n.274T>A
NM_001170634.1:c.897T>A	NP_001164105.1:p.Ser299=
NM_001170937.1:c.888T>A	NP_001164408.1:p.Ser296=
NM_004960.3:c.900T>A , LRG_655t1:c.900T>A	NP_004951.1:p.Ser300=
NR_028388.2:n.970T>A
XM_005255233.3:c.285T>A	XP_005255290.1:p.Ser95=
XM_011545781.1:c.894T>A	XP_011544083.1:p.Ser298=
XM_011545782.1:c.285T>A	XP_011544084.1:p.Ser95=
XM_005255233.5:c.285T>A	XP_005255290.1:p.Ser95=
XM_011545782.2:c.285T>A	XP_011544084.1:p.Ser95=
XM_024450221.1:c.891T>A	XP_024305989.1:p.Ser297=
NM_004960.4:c.900T>A MANE Select	NP_004951.1:p.Ser300=