Canonical Allele Identifier: CA395672461

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200531A>T (hg19) ; chr16:g.31189210A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189210A>T , CM000678.2:g.31189210A>T	GRCh38
NC_000016.9:g.31200531A>T , CM000678.1:g.31200531A>T	GRCh37
NC_000016.8:g.31108032A>T	NCBI36
NG_012889.2:g.14079A>T , LRG_655:g.14079A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.920A>T MANE Select	ENSP00000254108.8:p.Gln307Leu
ENST00000254108.11:c.920A>T	ENSP00000254108.7:p.Gln307Leu
ENST00000380244.7:c.917A>T	ENSP00000369594.3:p.Gln306Leu
ENST00000474990.5:n.214A>T
ENST00000487509.6:n.4095A>T
ENST00000564766.1:n.744A>T
ENST00000566605.5:c.*93A>T	ENSP00000455073.1:n.*93A>T
ENST00000568685.1:c.923A>T	ENSP00000455282.1:p.Gln308Leu
ENST00000568901.2:n.294A>T
NM_001170634.1:c.917A>T	NP_001164105.1:p.Gln306Leu
NM_001170937.1:c.908A>T	NP_001164408.1:p.Gln303Leu
NM_004960.3:c.920A>T , LRG_655t1:c.920A>T	NP_004951.1:p.Gln307Leu
NR_028388.2:n.990A>T
XM_005255233.3:c.305A>T	XP_005255290.1:p.Gln102Leu
XM_011545781.1:c.914A>T	XP_011544083.1:p.Gln305Leu
XM_011545782.1:c.305A>T	XP_011544084.1:p.Gln102Leu
XM_005255233.5:c.305A>T	XP_005255290.1:p.Gln102Leu
XM_011545782.2:c.305A>T	XP_011544084.1:p.Gln102Leu
XM_024450221.1:c.911A>T	XP_024305989.1:p.Gln304Leu
NM_004960.4:c.920A>T MANE Select	NP_004951.1:p.Gln307Leu