Canonical Allele Identifier: CA395677331

Gene: FUS

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191407A>C , CM000678.2:g.31191407A>C	GRCh38
NC_000016.9:g.31202728A>C , CM000678.1:g.31202728A>C	GRCh37
NC_000016.8:g.31110229A>C	NCBI36
NG_012889.2:g.16276A>C , LRG_655:g.16276A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.1550A>C MANE Select	ENSP00000254108.8:p.His517Pro
ENST00000254108.11:c.1550A>C	ENSP00000254108.7:p.His517Pro
ENST00000380244.7:c.1547A>C	ENSP00000369594.3:p.His516Pro
ENST00000483853.1:n.627A>C
ENST00000487509.6:n.4725A>C
ENST00000566605.5:c.*723A>C	ENSP00000455073.1:n.*723A>C
ENST00000568685.1:c.1553A>C	ENSP00000455282.1:p.His518Pro
ENST00000569760.5:n.441A>C
NM_001170634.1:c.1547A>C	NP_001164105.1:p.His516Pro
NM_001170937.1:c.1538A>C	NP_001164408.1:p.His513Pro
NM_004960.3:c.1550A>C , LRG_655t1:c.1550A>C	NP_004951.1:p.His517Pro
NR_028388.2:n.1620A>C
XM_005255233.3:c.935A>C	XP_005255290.1:p.His312Pro
XM_011545781.1:c.1544A>C	XP_011544083.1:p.His515Pro
XM_011545782.1:c.935A>C	XP_011544084.1:p.His312Pro
XM_005255233.5:c.935A>C	XP_005255290.1:p.His312Pro
XM_011545782.2:c.935A>C	XP_011544084.1:p.His312Pro
XM_024450221.1:c.1541A>C	XP_024305989.1:p.His514Pro
NM_004960.4:c.1550A>C MANE Select	NP_004951.1:p.His517Pro