Canonical Allele Identifier: CA2216944813

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185038A= , CM000678.2:g.31185038A=	GRCh38
NC_000016.9:g.31196359A= , CM000678.1:g.31196359A=	GRCh37
NC_000016.8:g.31103860A=	NCBI36
NG_012889.2:g.9907A= , LRG_655:g.9907A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.623A= MANE Select	ENSP00000254108.8:p.Tyr208=
ENST00000254108.11:c.623A=	ENSP00000254108.7:p.Tyr208=
ENST00000380244.7:c.620A=	ENSP00000369594.3:p.Tyr207=
ENST00000487509.6:n.688A=
ENST00000566605.5:c.623A=	ENSP00000455073.1:p.Tyr208=
ENST00000568685.1:c.623A=	ENSP00000455282.1:p.Tyr208=
NM_001170634.1:c.620A=	NP_001164105.1:p.Tyr207=
NM_001170937.1:c.611A=	NP_001164408.1:p.Tyr204=
NM_004960.3:c.623A= , LRG_655t1:c.623A=	NP_004951.1:p.Tyr208=
NR_028388.2:n.728A=
XM_005255233.3:c.43A=	XP_005255290.1:p.Met15=
XM_011545781.1:c.617A=	XP_011544083.1:p.Tyr206=
XM_011545782.1:c.43A=	XP_011544084.1:p.Met15=
XM_005255233.5:c.43A=	XP_005255290.1:p.Met15=
XM_011545782.2:c.43A=	XP_011544084.1:p.Met15=
XM_024450221.1:c.614A=	XP_024305989.1:p.Tyr205=
NM_004960.4:c.623A= MANE Select	NP_004951.1:p.Tyr208=