Canonical Allele Identifier: CA621871799

Gene: FUS

Linked Data

• dbSNP Id: rs929867
• gnomAD v2: 16-31191482-A-T
• gnomAD v3: 16-31180161-A-T
• gnomAD v4: 16-31180161-A-T
• MyVariant Identifiers: chr16:g.31191482A>T (hg19) ; chr16:g.31180161A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31180161A>T , CM000678.2:g.31180161A>T	GRCh38
NC_000016.9:g.31191482A>T , CM000678.1:g.31191482A>T	GRCh37
NC_000016.8:g.31098983A>T	NCBI36
NG_012889.2:g.5030A>T , LRG_655:g.5030A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.-54A>T MANE Select	ENSP00000254108.8:n.-54A>T
ENST00000254108.11:c.-54A>T	ENSP00000254108.7:n.-54A>T
ENST00000380244.7:c.-54A>T	ENSP00000369594.3:n.-54A>T
ENST00000487045.6:n.23A>T
ENST00000487509.6:n.12A>T
ENST00000566605.5:c.-54A>T	ENSP00000455073.1:n.-54A>T
ENST00000568685.1:c.-54A>T	ENSP00000455282.1:n.-54A>T
NM_001170634.1:c.-54A>T	NP_001164105.1:n.-54A>T
NM_001170937.1:c.-54A>T	NP_001164408.1:n.-54A>T
NM_004960.3:c.-54A>T , LRG_655t1:c.-54A>T	NP_004951.1:n.-54A>T
NR_028388.2:n.52A>T
XM_005255233.3:c.-631A>T	XP_005255290.1:n.-631A>T
XM_011545781.1:c.-54A>T	XP_011544083.1:n.-54A>T
XM_005255233.5:c.-631A>T	XP_005255290.1:n.-631A>T
XM_024450221.1:c.-54A>T	XP_024305989.1:n.-54A>T
NM_004960.4:c.-54A>T MANE Select	NP_004951.1:n.-54A>T