Canonical Allele Identifier: CA395672552
Gene: FUS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.31189225A>G , CM000678.2:g.31189225A>G GRCh38
NC_000016.9:g.31200546A>G , CM000678.1:g.31200546A>G GRCh37
NC_000016.8:g.31108047A>G NCBI36
NG_012889.2:g.14094A>G , LRG_655:g.14094A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254108.12:c.935A>G MANE Select ENSP00000254108.8:p.Lys312Arg
ENST00000254108.11:c.935A>G ENSP00000254108.7:p.Lys312Arg
ENST00000380244.7:c.932A>G ENSP00000369594.3:p.Lys311Arg
ENST00000474990.5:n.229A>G
ENST00000487509.6:n.4110A>G
ENST00000564766.1:n.759A>G
ENST00000566605.5:c.*108A>G ENSP00000455073.1:n.*108A>G
ENST00000568685.1:c.938A>G ENSP00000455282.1:p.Lys313Arg
ENST00000568901.2:n.309A>G
NM_001170634.1:c.932A>G NP_001164105.1:p.Lys311Arg
NM_001170937.1:c.923A>G NP_001164408.1:p.Lys308Arg
NM_004960.3:c.935A>G , LRG_655t1:c.935A>G NP_004951.1:p.Lys312Arg
NR_028388.2:n.1005A>G
XM_005255233.3:c.320A>G XP_005255290.1:p.Lys107Arg
XM_011545781.1:c.929A>G XP_011544083.1:p.Lys310Arg
XM_011545782.1:c.320A>G XP_011544084.1:p.Lys107Arg
XM_005255233.5:c.320A>G XP_005255290.1:p.Lys107Arg
XM_011545782.2:c.320A>G XP_011544084.1:p.Lys107Arg
XM_024450221.1:c.926A>G XP_024305989.1:p.Lys309Arg
NM_004960.4:c.935A>G MANE Select NP_004951.1:p.Lys312Arg