Canonical Allele Identifier: CA494713682

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200502A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189181A>G , CM000678.2:g.31189181A>G	GRCh38
NC_000016.9:g.31200502A>G , CM000678.1:g.31200502A>G	GRCh37
NC_000016.8:g.31108003A>G	NCBI36
NG_012889.2:g.14050A>G , LRG_655:g.14050A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.891A>G MANE Select	ENSP00000254108.8:p.Thr297=
ENST00000254108.11:c.891A>G	ENSP00000254108.7:p.Thr297=
ENST00000380244.7:c.888A>G	ENSP00000369594.3:p.Thr296=
ENST00000474990.5:n.185A>G
ENST00000487509.6:n.4066A>G
ENST00000564766.1:n.715A>G
ENST00000566605.5:c.*64A>G	ENSP00000455073.1:n.*64A>G
ENST00000568685.1:c.894A>G	ENSP00000455282.1:p.Thr298=
ENST00000568901.2:n.265A>G
NM_001170634.1:c.888A>G	NP_001164105.1:p.Thr296=
NM_001170937.1:c.879A>G	NP_001164408.1:p.Thr293=
NM_004960.3:c.891A>G , LRG_655t1:c.891A>G	NP_004951.1:p.Thr297=
NR_028388.2:n.961A>G
XM_005255233.3:c.276A>G	XP_005255290.1:p.Thr92=
XM_011545781.1:c.885A>G	XP_011544083.1:p.Thr295=
XM_011545782.1:c.276A>G	XP_011544084.1:p.Thr92=
XM_005255233.5:c.276A>G	XP_005255290.1:p.Thr92=
XM_011545782.2:c.276A>G	XP_011544084.1:p.Thr92=
XM_024450221.1:c.882A>G	XP_024305989.1:p.Thr294=
NM_004960.4:c.891A>G MANE Select	NP_004951.1:p.Thr297=