Canonical Allele Identifier: CA494928772

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196369G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185048G>A , CM000678.2:g.31185048G>A	GRCh38
NC_000016.9:g.31196369G>A , CM000678.1:g.31196369G>A	GRCh37
NC_000016.8:g.31103870G>A	NCBI36
NG_012889.2:g.9917G>A , LRG_655:g.9917G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.633G>A MANE Select	ENSP00000254108.8:p.Gln211=
ENST00000254108.11:c.633G>A	ENSP00000254108.7:p.Gln211=
ENST00000380244.7:c.630G>A	ENSP00000369594.3:p.Gln210=
ENST00000487509.6:n.698G>A
ENST00000566605.5:c.633G>A	ENSP00000455073.1:p.Gln211=
ENST00000568685.1:c.633G>A	ENSP00000455282.1:p.Gln211=
NM_001170634.1:c.630G>A	NP_001164105.1:p.Gln210=
NM_001170937.1:c.621G>A	NP_001164408.1:p.Gln207=
NM_004960.3:c.633G>A , LRG_655t1:c.633G>A	NP_004951.1:p.Gln211=
NR_028388.2:n.738G>A
XM_005255233.3:c.53G>A	XP_005255290.1:p.Arg18Lys
XM_011545781.1:c.627G>A	XP_011544083.1:p.Gln209=
XM_011545782.1:c.53G>A	XP_011544084.1:p.Arg18Lys
XM_005255233.5:c.53G>A	XP_005255290.1:p.Arg18Lys
XM_011545782.2:c.53G>A	XP_011544084.1:p.Arg18Lys
XM_024450221.1:c.624G>A	XP_024305989.1:p.Gln208=
NM_004960.4:c.633G>A MANE Select	NP_004951.1:p.Gln211=