Canonical Allele Identifier: CA494928666

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184988T>G , CM000678.2:g.31184988T>G	GRCh38
NC_000016.9:g.31196309T>G , CM000678.1:g.31196309T>G	GRCh37
NC_000016.8:g.31103810T>G	NCBI36
NG_012889.2:g.9857T>G , LRG_655:g.9857T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.573T>G MANE Select	NP_004951.1:p.Gly191=
ENST00000254108.12:c.573T>G MANE Select	ENSP00000254108.8:p.Gly191=
NM_001170634.1:c.570T>G	NP_001164105.1:p.Gly190=
NM_001170937.1:c.561T>G	NP_001164408.1:p.Gly187=
NM_004960.3:c.573T>G , LRG_655t1:c.573T>G	NP_004951.1:p.Gly191=
NR_028388.2:n.678T>G
ENST00000254108.11:c.573T>G	ENSP00000254108.7:p.Gly191=
ENST00000380244.7:c.570T>G	ENSP00000369594.3:p.Gly190=
ENST00000487509.6:n.638T>G
ENST00000566605.5:c.573T>G	ENSP00000455073.1:p.Gly191=
ENST00000568685.1:c.573T>G	ENSP00000455282.1:p.Gly191=
XM_005255233.3:c.-8T>G	XP_005255290.1:n.-8T>G
XM_005255233.5:c.-8T>G	XP_005255290.1:n.-8T>G
XM_011545781.1:c.567T>G	XP_011544083.1:p.Gly189=
XM_011545782.1:c.-8T>G	XP_011544084.1:n.-8T>G
XM_011545782.2:c.-8T>G	XP_011544084.1:n.-8T>G
XM_024450221.1:c.564T>G	XP_024305989.1:p.Gly188=