Canonical Allele Identifier: CA2216947141

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189087C= , CM000678.2:g.31189087C=	GRCh38
NC_000016.9:g.31200408C= , CM000678.1:g.31200408C=	GRCh37
NC_000016.8:g.31107909C=	NCBI36
NG_012889.2:g.13956C= , LRG_655:g.13956C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.833-36C= MANE Select	ENSP00000254108.8:n.833-36C=
ENST00000254108.11:c.833-36C=	ENSP00000254108.7:n.833-36C=
ENST00000380244.7:c.830-36C=	ENSP00000369594.3:n.830-36C=
ENST00000474990.5:n.127-36C=
ENST00000487509.6:n.4008-36C=
ENST00000564766.1:n.621C=
ENST00000566605.5:c.*6-36C=	ENSP00000455073.1:n.*6-36C=
ENST00000568685.1:c.833-33C=	ENSP00000455282.1:n.833-33C=
ENST00000568901.2:n.207-36C=
NM_001170634.1:c.830-36C=	NP_001164105.1:n.830-36C=
NM_001170937.1:c.821-36C=	NP_001164408.1:n.821-36C=
NM_004960.3:c.833-36C= , LRG_655t1:c.833-36C=	NP_004951.1:n.833-36C=
NR_028388.2:n.903-36C=
XM_005255233.3:c.218-36C=	XP_005255290.1:n.218-36C=
XM_011545781.1:c.827-36C=	XP_011544083.1:n.827-36C=
XM_011545782.1:c.218-36C=	XP_011544084.1:n.218-36C=
XM_005255233.5:c.218-36C=	XP_005255290.1:n.218-36C=
XM_011545782.2:c.218-36C=	XP_011544084.1:n.218-36C=
XM_024450221.1:c.824-36C=	XP_024305989.1:n.824-36C=
NM_004960.4:c.833-36C= MANE Select	NP_004951.1:n.833-36C=