Canonical Allele Identifier: CA8023718
Community Standard Title: NM_004960.4(FUS):c.613A>G (p.Ser205Gly)
Gene: FUS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31185028A>G , CM000678.2:g.31185028A>G GRCh38
NC_000016.9:g.31196349A>G , CM000678.1:g.31196349A>G GRCh37
NC_000016.8:g.31103850A>G NCBI36
NG_012889.2:g.9897A>G , LRG_655:g.9897A>G

Transcript Alleles

HGVS Amino-acid Change
NM_004960.4:c.613A>G MANE Select NP_004951.1:p.Ser205Gly
ENST00000254108.12:c.613A>G MANE Select ENSP00000254108.8:p.Ser205Gly
NM_001170634.1:c.610A>G NP_001164105.1:p.Ser204Gly
NM_001170937.1:c.601A>G NP_001164408.1:p.Ser201Gly
NM_004960.3:c.613A>G , LRG_655t1:c.613A>G NP_004951.1:p.Ser205Gly
NR_028388.2:n.718A>G
ENST00000254108.11:c.613A>G ENSP00000254108.7:p.Ser205Gly
ENST00000380244.7:c.610A>G ENSP00000369594.3:p.Ser204Gly
ENST00000487509.6:n.678A>G
ENST00000566605.5:c.613A>G ENSP00000455073.1:p.Ser205Gly
ENST00000568685.1:c.613A>G ENSP00000455282.1:p.Ser205Gly
XM_005255233.3:c.33A>G XP_005255290.1:p.Ala11=
XM_005255233.5:c.33A>G XP_005255290.1:p.Ala11=
XM_011545781.1:c.607A>G XP_011544083.1:p.Ser203Gly
XM_011545782.1:c.33A>G XP_011544084.1:p.Ala11=
XM_011545782.2:c.33A>G XP_011544084.1:p.Ala11=
XM_024450221.1:c.604A>G XP_024305989.1:p.Ser202Gly