Canonical Allele Identifier: CA395669701

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196317A>G (hg19) ; chr16:g.31184996A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184996A>G , CM000678.2:g.31184996A>G	GRCh38
NC_000016.9:g.31196317A>G , CM000678.1:g.31196317A>G	GRCh37
NC_000016.8:g.31103818A>G	NCBI36
NG_012889.2:g.9865A>G , LRG_655:g.9865A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.581A>G MANE Select	ENSP00000254108.8:p.Tyr194Cys
ENST00000254108.11:c.581A>G	ENSP00000254108.7:p.Tyr194Cys
ENST00000380244.7:c.578A>G	ENSP00000369594.3:p.Tyr193Cys
ENST00000487509.6:n.646A>G
ENST00000566605.5:c.581A>G	ENSP00000455073.1:p.Tyr194Cys
ENST00000568685.1:c.581A>G	ENSP00000455282.1:p.Tyr194Cys
NM_001170634.1:c.578A>G	NP_001164105.1:p.Tyr193Cys
NM_001170937.1:c.569A>G	NP_001164408.1:p.Tyr190Cys
NM_004960.3:c.581A>G , LRG_655t1:c.581A>G	NP_004951.1:p.Tyr194Cys
NR_028388.2:n.686A>G
XM_005255233.3:c.1A>G	XP_005255290.1:p.Met1Val
XM_011545781.1:c.575A>G	XP_011544083.1:p.Tyr192Cys
XM_011545782.1:c.1A>G	XP_011544084.1:p.Met1Val
XM_005255233.5:c.1A>G	XP_005255290.1:p.Met1Val
XM_011545782.2:c.1A>G	XP_011544084.1:p.Met1Val
XM_024450221.1:c.572A>G	XP_024305989.1:p.Tyr191Cys
NM_004960.4:c.581A>G MANE Select	NP_004951.1:p.Tyr194Cys