Canonical Allele Identifier: CA395672369

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200516C>G (hg19) ; chr16:g.31189195C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189195C>G , CM000678.2:g.31189195C>G	GRCh38
NC_000016.9:g.31200516C>G , CM000678.1:g.31200516C>G	GRCh37
NC_000016.8:g.31108017C>G	NCBI36
NG_012889.2:g.14064C>G , LRG_655:g.14064C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.905C>G MANE Select	ENSP00000254108.8:p.Ala302Gly
ENST00000254108.11:c.905C>G	ENSP00000254108.7:p.Ala302Gly
ENST00000380244.7:c.902C>G	ENSP00000369594.3:p.Ala301Gly
ENST00000474990.5:n.199C>G
ENST00000487509.6:n.4080C>G
ENST00000564766.1:n.729C>G
ENST00000566605.5:c.*78C>G	ENSP00000455073.1:n.*78C>G
ENST00000568685.1:c.908C>G	ENSP00000455282.1:p.Ala303Gly
ENST00000568901.2:n.279C>G
NM_001170634.1:c.902C>G	NP_001164105.1:p.Ala301Gly
NM_001170937.1:c.893C>G	NP_001164408.1:p.Ala298Gly
NM_004960.3:c.905C>G , LRG_655t1:c.905C>G	NP_004951.1:p.Ala302Gly
NR_028388.2:n.975C>G
XM_005255233.3:c.290C>G	XP_005255290.1:p.Ala97Gly
XM_011545781.1:c.899C>G	XP_011544083.1:p.Ala300Gly
XM_011545782.1:c.290C>G	XP_011544084.1:p.Ala97Gly
XM_005255233.5:c.290C>G	XP_005255290.1:p.Ala97Gly
XM_011545782.2:c.290C>G	XP_011544084.1:p.Ala97Gly
XM_024450221.1:c.896C>G	XP_024305989.1:p.Ala299Gly
NM_004960.4:c.905C>G MANE Select	NP_004951.1:p.Ala302Gly