Canonical Allele Identifier: CA280594678
Gene: FUS HGNC NCBI

Linked Data

ClinVar Variation Id: 956175
ClinVar RCV Id: RCV001228930
dbSNP Id: rs148758737

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31184986G>A , CM000678.2:g.31184986G>A GRCh38
NC_000016.9:g.31196307G>A , CM000678.1:g.31196307G>A GRCh37
NC_000016.8:g.31103808G>A NCBI36
NG_012889.2:g.9855G>A , LRG_655:g.9855G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.571G>A MANE Select ENSP00000254108.8:p.Gly191Ser
ENST00000254108.11:c.571G>A ENSP00000254108.7:p.Gly191Ser
ENST00000380244.7:c.568G>A ENSP00000369594.3:p.Gly190Ser
ENST00000487509.6:n.636G>A
ENST00000566605.5:c.571G>A ENSP00000455073.1:p.Gly191Ser
ENST00000568685.1:c.571G>A ENSP00000455282.1:p.Gly191Ser
NM_001170634.1:c.568G>A NP_001164105.1:p.Gly190Ser
NM_001170937.1:c.559G>A NP_001164408.1:p.Gly187Ser
NM_004960.3:c.571G>A , LRG_655t1:c.571G>A NP_004951.1:p.Gly191Ser
NR_028388.2:n.676G>A
XM_005255233.3:c.-10G>A XP_005255290.1:n.-10G>A
XM_011545781.1:c.565G>A XP_011544083.1:p.Gly189Ser
XM_011545782.1:c.-10G>A XP_011544084.1:n.-10G>A
XM_005255233.5:c.-10G>A XP_005255290.1:n.-10G>A
XM_011545782.2:c.-10G>A XP_011544084.1:n.-10G>A
XM_024450221.1:c.562G>A XP_024305989.1:p.Gly188Ser
NM_004960.4:c.571G>A MANE Select NP_004951.1:p.Gly191Ser