Canonical Allele Identifier: CA8023323

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31180168G>A , CM000678.2:g.31180168G>A	GRCh38
NC_000016.9:g.31191489G>A , CM000678.1:g.31191489G>A	GRCh37
NC_000016.8:g.31098990G>A	NCBI36
NG_012889.2:g.5037G>A , LRG_655:g.5037G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.-47G>A MANE Select	NP_004951.1:n.-47G>A
ENST00000254108.12:c.-47G>A MANE Select	ENSP00000254108.8:n.-47G>A
NM_001170634.1:c.-47G>A	NP_001164105.1:n.-47G>A
NM_001170937.1:c.-47G>A	NP_001164408.1:n.-47G>A
NM_004960.3:c.-47G>A , LRG_655t1:c.-47G>A	NP_004951.1:n.-47G>A
NR_028388.2:n.59G>A
ENST00000254108.11:c.-47G>A	ENSP00000254108.7:n.-47G>A
ENST00000380244.7:c.-47G>A	ENSP00000369594.3:n.-47G>A
ENST00000487045.6:n.30G>A
ENST00000487509.6:n.19G>A
ENST00000566605.5:c.-47G>A	ENSP00000455073.1:n.-47G>A
ENST00000568685.1:c.-47G>A	ENSP00000455282.1:n.-47G>A
XM_005255233.3:c.-624G>A	XP_005255290.1:n.-624G>A
XM_005255233.5:c.-624G>A	XP_005255290.1:n.-624G>A
XM_011545781.1:c.-47G>A	XP_011544083.1:n.-47G>A
XM_024450221.1:c.-47G>A	XP_024305989.1:n.-47G>A