Canonical Allele Identifier: CA2216948320

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191360A= , CM000678.2:g.31191360A=	GRCh38
NC_000016.9:g.31202681A= , CM000678.1:g.31202681A=	GRCh37
NC_000016.8:g.31110182A=	NCBI36
NG_012889.2:g.16229A= , LRG_655:g.16229A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.1542-39A= MANE Select	ENSP00000254108.8:n.1542-39A=
ENST00000254108.11:c.1542-39A=	ENSP00000254108.7:n.1542-39A=
ENST00000380244.7:c.1539-39A=	ENSP00000369594.3:n.1539-39A=
ENST00000483853.1:n.619-39A=
ENST00000487509.6:n.4717-39A=
ENST00000566605.5:c.*715-39A=	ENSP00000455073.1:n.*715-39A=
ENST00000568685.1:c.1545-39A=	ENSP00000455282.1:n.1545-39A=
ENST00000569760.5:n.433-39A=
NM_001170634.1:c.1539-39A=	NP_001164105.1:n.1539-39A=
NM_001170937.1:c.1530-39A=	NP_001164408.1:n.1530-39A=
NM_004960.3:c.1542-39A= , LRG_655t1:c.1542-39A=	NP_004951.1:n.1542-39A=
NR_028388.2:n.1612-39A=
XM_005255233.3:c.927-39A=	XP_005255290.1:n.927-39A=
XM_011545781.1:c.1536-39A=	XP_011544083.1:n.1536-39A=
XM_011545782.1:c.927-39A=	XP_011544084.1:n.927-39A=
XM_005255233.5:c.927-39A=	XP_005255290.1:n.927-39A=
XM_011545782.2:c.927-39A=	XP_011544084.1:n.927-39A=
XM_024450221.1:c.1533-39A=	XP_024305989.1:n.1533-39A=
NM_004960.4:c.1542-39A= MANE Select	NP_004951.1:n.1542-39A=