Canonical Allele Identifier: CA494928739

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196348C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185027C>G , CM000678.2:g.31185027C>G	GRCh38
NC_000016.9:g.31196348C>G , CM000678.1:g.31196348C>G	GRCh37
NC_000016.8:g.31103849C>G	NCBI36
NG_012889.2:g.9896C>G , LRG_655:g.9896C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.612C>G MANE Select	ENSP00000254108.8:p.Gly204=
ENST00000254108.11:c.612C>G	ENSP00000254108.7:p.Gly204=
ENST00000380244.7:c.609C>G	ENSP00000369594.3:p.Gly203=
ENST00000487509.6:n.677C>G
ENST00000566605.5:c.612C>G	ENSP00000455073.1:p.Gly204=
ENST00000568685.1:c.612C>G	ENSP00000455282.1:p.Gly204=
NM_001170634.1:c.609C>G	NP_001164105.1:p.Gly203=
NM_001170937.1:c.600C>G	NP_001164408.1:p.Gly200=
NM_004960.3:c.612C>G , LRG_655t1:c.612C>G	NP_004951.1:p.Gly204=
NR_028388.2:n.717C>G
XM_005255233.3:c.32C>G	XP_005255290.1:p.Ala11Gly
XM_011545781.1:c.606C>G	XP_011544083.1:p.Gly202=
XM_011545782.1:c.32C>G	XP_011544084.1:p.Ala11Gly
XM_005255233.5:c.32C>G	XP_005255290.1:p.Ala11Gly
XM_011545782.2:c.32C>G	XP_011544084.1:p.Ala11Gly
XM_024450221.1:c.603C>G	XP_024305989.1:p.Gly201=
NM_004960.4:c.612C>G MANE Select	NP_004951.1:p.Gly204=