Canonical Allele Identifier: CA8023840

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31188356C>T , CM000678.2:g.31188356C>T	GRCh38
NC_000016.9:g.31199677C>T , CM000678.1:g.31199677C>T	GRCh37
NC_000016.8:g.31107178C>T	NCBI36
NG_012889.2:g.13225C>T , LRG_655:g.13225C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.831C>T MANE Select	NP_004951.1:p.Ser277=
ENST00000254108.12:c.831C>T MANE Select	ENSP00000254108.8:p.Ser277=
NM_001170634.1:c.828C>T	NP_001164105.1:p.Ser276=
NM_001170937.1:c.819C>T	NP_001164408.1:p.Ser273=
NM_004960.3:c.831C>T , LRG_655t1:c.831C>T	NP_004951.1:p.Ser277=
NR_028388.2:n.901C>T
ENST00000254108.11:c.831C>T	ENSP00000254108.7:p.Ser277=
ENST00000380244.7:c.828C>T	ENSP00000369594.3:p.Ser276=
ENST00000474990.5:n.125C>T
ENST00000487509.6:n.4006C>T
ENST00000566605.5:c.*4C>T	ENSP00000455073.1:n.*4C>T
ENST00000568685.1:c.831C>T	ENSP00000455282.1:p.Ser277=
ENST00000568901.2:n.205C>T
XM_005255233.3:c.216C>T	XP_005255290.1:p.Ser72=
XM_005255233.5:c.216C>T	XP_005255290.1:p.Ser72=
XM_011545781.1:c.825C>T	XP_011544083.1:p.Ser275=
XM_011545782.1:c.216C>T	XP_011544084.1:p.Ser72=
XM_011545782.2:c.216C>T	XP_011544084.1:p.Ser72=
XM_024450221.1:c.822C>T	XP_024305989.1:p.Ser274=