Canonical Allele Identifier: CA8023557

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183940C>T , CM000678.2:g.31183940C>T	GRCh38
NC_000016.9:g.31195261C>T , CM000678.1:g.31195261C>T	GRCh37
NC_000016.8:g.31102762C>T	NCBI36
NG_012889.2:g.8809C>T , LRG_655:g.8809C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.273C>T MANE Select	NP_004951.1:p.Tyr91=
ENST00000254108.12:c.273C>T MANE Select	ENSP00000254108.8:p.Tyr91=
NM_001170634.1:c.270C>T	NP_001164105.1:p.Tyr90=
NM_001170937.1:c.273C>T	NP_001164408.1:p.Tyr91=
NM_004960.3:c.273C>T , LRG_655t1:c.273C>T	NP_004951.1:p.Tyr91=
NR_028388.2:n.378C>T
ENST00000254108.11:c.273C>T	ENSP00000254108.7:p.Tyr91=
ENST00000380244.7:c.270C>T	ENSP00000369594.3:p.Tyr90=
ENST00000487509.6:n.338C>T
ENST00000487974.1:n.391C>T
ENST00000566605.5:c.273C>T	ENSP00000455073.1:p.Tyr91=
ENST00000568685.1:c.273C>T	ENSP00000455282.1:p.Tyr91=
XM_005255233.3:c.-308C>T	XP_005255290.1:n.-308C>T
XM_005255233.5:c.-308C>T	XP_005255290.1:n.-308C>T
XM_011545781.1:c.273C>T	XP_011544083.1:p.Tyr91=
XM_024450221.1:c.270C>T	XP_024305989.1:p.Tyr90=