Canonical Allele Identifier: CA494928654

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196300T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184979T>G , CM000678.2:g.31184979T>G	GRCh38
NC_000016.9:g.31196300T>G , CM000678.1:g.31196300T>G	GRCh37
NC_000016.8:g.31103801T>G	NCBI36
NG_012889.2:g.9848T>G , LRG_655:g.9848T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.564T>G MANE Select	ENSP00000254108.8:p.Gly188=
ENST00000254108.11:c.564T>G	ENSP00000254108.7:p.Gly188=
ENST00000380244.7:c.561T>G	ENSP00000369594.3:p.Gly187=
ENST00000487509.6:n.629T>G
ENST00000566605.5:c.564T>G	ENSP00000455073.1:p.Gly188=
ENST00000568685.1:c.564T>G	ENSP00000455282.1:p.Gly188=
NM_001170634.1:c.561T>G	NP_001164105.1:p.Gly187=
NM_001170937.1:c.552T>G	NP_001164408.1:p.Gly184=
NM_004960.3:c.564T>G , LRG_655t1:c.564T>G	NP_004951.1:p.Gly188=
NR_028388.2:n.669T>G
XM_005255233.3:c.-17T>G	XP_005255290.1:n.-17T>G
XM_011545781.1:c.558T>G	XP_011544083.1:p.Gly186=
XM_011545782.1:c.-17T>G	XP_011544084.1:n.-17T>G
XM_005255233.5:c.-17T>G	XP_005255290.1:n.-17T>G
XM_011545782.2:c.-17T>G	XP_011544084.1:n.-17T>G
XM_024450221.1:c.555T>G	XP_024305989.1:p.Gly185=
NM_004960.4:c.564T>G MANE Select	NP_004951.1:p.Gly188=