Canonical Allele Identifier: CA494710650

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31195192T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183871T>A , CM000678.2:g.31183871T>A	GRCh38
NC_000016.9:g.31195192T>A , CM000678.1:g.31195192T>A	GRCh37
NC_000016.8:g.31102693T>A	NCBI36
NG_012889.2:g.8740T>A , LRG_655:g.8740T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.204T>A MANE Select	ENSP00000254108.8:p.Thr68=
ENST00000254108.11:c.204T>A	ENSP00000254108.7:p.Thr68=
ENST00000380244.7:c.201T>A	ENSP00000369594.3:p.Thr67=
ENST00000487509.6:n.269T>A
ENST00000487974.1:n.322T>A
ENST00000566605.5:c.204T>A	ENSP00000455073.1:p.Thr68=
ENST00000568685.1:c.204T>A	ENSP00000455282.1:p.Thr68=
NM_001170634.1:c.201T>A	NP_001164105.1:p.Thr67=
NM_001170937.1:c.204T>A	NP_001164408.1:p.Thr68=
NM_004960.3:c.204T>A , LRG_655t1:c.204T>A	NP_004951.1:p.Thr68=
NR_028388.2:n.309T>A
XM_005255233.3:c.-377T>A	XP_005255290.1:n.-377T>A
XM_011545781.1:c.204T>A	XP_011544083.1:p.Thr68=
XM_005255233.5:c.-377T>A	XP_005255290.1:n.-377T>A
XM_024450221.1:c.201T>A	XP_024305989.1:p.Thr67=
NM_004960.4:c.204T>A MANE Select	NP_004951.1:p.Thr68=