Canonical Allele Identifier: CA395672159

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200483G>T (hg19) ; chr16:g.31189162G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189162G>T , CM000678.2:g.31189162G>T	GRCh38
NC_000016.9:g.31200483G>T , CM000678.1:g.31200483G>T	GRCh37
NC_000016.8:g.31107984G>T	NCBI36
NG_012889.2:g.14031G>T , LRG_655:g.14031G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.872G>T MANE Select	ENSP00000254108.8:p.Gly291Val
ENST00000254108.11:c.872G>T	ENSP00000254108.7:p.Gly291Val
ENST00000380244.7:c.869G>T	ENSP00000369594.3:p.Gly290Val
ENST00000474990.5:n.166G>T
ENST00000487509.6:n.4047G>T
ENST00000564766.1:n.696G>T
ENST00000566605.5:c.*45G>T	ENSP00000455073.1:n.*45G>T
ENST00000568685.1:c.875G>T	ENSP00000455282.1:p.Gly292Val
ENST00000568901.2:n.246G>T
NM_001170634.1:c.869G>T	NP_001164105.1:p.Gly290Val
NM_001170937.1:c.860G>T	NP_001164408.1:p.Gly287Val
NM_004960.3:c.872G>T , LRG_655t1:c.872G>T	NP_004951.1:p.Gly291Val
NR_028388.2:n.942G>T
XM_005255233.3:c.257G>T	XP_005255290.1:p.Gly86Val
XM_011545781.1:c.866G>T	XP_011544083.1:p.Gly289Val
XM_011545782.1:c.257G>T	XP_011544084.1:p.Gly86Val
XM_005255233.5:c.257G>T	XP_005255290.1:p.Gly86Val
XM_011545782.2:c.257G>T	XP_011544084.1:p.Gly86Val
XM_024450221.1:c.863G>T	XP_024305989.1:p.Gly288Val
NM_004960.4:c.872G>T MANE Select	NP_004951.1:p.Gly291Val