Canonical Allele Identifier: CA395669566

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196277C>A (hg19) ; chr16:g.31184956C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184956C>A , CM000678.2:g.31184956C>A	GRCh38
NC_000016.9:g.31196277C>A , CM000678.1:g.31196277C>A	GRCh37
NC_000016.8:g.31103778C>A	NCBI36
NG_012889.2:g.9825C>A , LRG_655:g.9825C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.541C>A MANE Select	ENSP00000254108.8:p.Gln181Lys
ENST00000254108.11:c.541C>A	ENSP00000254108.7:p.Gln181Lys
ENST00000380244.7:c.538C>A	ENSP00000369594.3:p.Gln180Lys
ENST00000487509.6:n.606C>A
ENST00000566605.5:c.541C>A	ENSP00000455073.1:p.Gln181Lys
ENST00000568685.1:c.541C>A	ENSP00000455282.1:p.Gln181Lys
NM_001170634.1:c.538C>A	NP_001164105.1:p.Gln180Lys
NM_001170937.1:c.529C>A	NP_001164408.1:p.Gln177Lys
NM_004960.3:c.541C>A , LRG_655t1:c.541C>A	NP_004951.1:p.Gln181Lys
NR_028388.2:n.646C>A
XM_005255233.3:c.-40C>A	XP_005255290.1:n.-40C>A
XM_011545781.1:c.535C>A	XP_011544083.1:p.Gln179Lys
XM_011545782.1:c.-40C>A	XP_011544084.1:n.-40C>A
XM_005255233.5:c.-40C>A	XP_005255290.1:n.-40C>A
XM_011545782.2:c.-40C>A	XP_011544084.1:n.-40C>A
XM_024450221.1:c.532C>A	XP_024305989.1:p.Gln178Lys
NM_004960.4:c.541C>A MANE Select	NP_004951.1:p.Gln181Lys