Canonical Allele Identifier: CA2216947129

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189071G= , CM000678.2:g.31189071G=	GRCh38
NC_000016.9:g.31200392G= , CM000678.1:g.31200392G=	GRCh37
NC_000016.8:g.31107893G=	NCBI36
NG_012889.2:g.13940G= , LRG_655:g.13940G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.833-52G= MANE Select	ENSP00000254108.8:n.833-52G=
ENST00000254108.11:c.833-52G=	ENSP00000254108.7:n.833-52G=
ENST00000380244.7:c.830-52G=	ENSP00000369594.3:n.830-52G=
ENST00000474990.5:n.127-52G=
ENST00000487509.6:n.4008-52G=
ENST00000564766.1:n.605G=
ENST00000566605.5:c.*6-52G=	ENSP00000455073.1:n.*6-52G=
ENST00000568685.1:c.833-49G=	ENSP00000455282.1:n.833-49G=
ENST00000568901.2:n.207-52G=
NM_001170634.1:c.830-52G=	NP_001164105.1:n.830-52G=
NM_001170937.1:c.821-52G=	NP_001164408.1:n.821-52G=
NM_004960.3:c.833-52G= , LRG_655t1:c.833-52G=	NP_004951.1:n.833-52G=
NR_028388.2:n.903-52G=
XM_005255233.3:c.218-52G=	XP_005255290.1:n.218-52G=
XM_011545781.1:c.827-52G=	XP_011544083.1:n.827-52G=
XM_011545782.1:c.218-52G=	XP_011544084.1:n.218-52G=
XM_005255233.5:c.218-52G=	XP_005255290.1:n.218-52G=
XM_011545782.2:c.218-52G=	XP_011544084.1:n.218-52G=
XM_024450221.1:c.824-52G=	XP_024305989.1:n.824-52G=
NM_004960.4:c.833-52G= MANE Select	NP_004951.1:n.833-52G=