Canonical Allele Identifier: CA494713716

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200529G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189208G>A , CM000678.2:g.31189208G>A	GRCh38
NC_000016.9:g.31200529G>A , CM000678.1:g.31200529G>A	GRCh37
NC_000016.8:g.31108030G>A	NCBI36
NG_012889.2:g.14077G>A , LRG_655:g.14077G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.918G>A MANE Select	ENSP00000254108.8:p.Lys306=
ENST00000254108.11:c.918G>A	ENSP00000254108.7:p.Lys306=
ENST00000380244.7:c.915G>A	ENSP00000369594.3:p.Lys305=
ENST00000474990.5:n.212G>A
ENST00000487509.6:n.4093G>A
ENST00000564766.1:n.742G>A
ENST00000566605.5:c.*91G>A	ENSP00000455073.1:n.*91G>A
ENST00000568685.1:c.921G>A	ENSP00000455282.1:p.Lys307=
ENST00000568901.2:n.292G>A
NM_001170634.1:c.915G>A	NP_001164105.1:p.Lys305=
NM_001170937.1:c.906G>A	NP_001164408.1:p.Lys302=
NM_004960.3:c.918G>A , LRG_655t1:c.918G>A	NP_004951.1:p.Lys306=
NR_028388.2:n.988G>A
XM_005255233.3:c.303G>A	XP_005255290.1:p.Lys101=
XM_011545781.1:c.912G>A	XP_011544083.1:p.Lys304=
XM_011545782.1:c.303G>A	XP_011544084.1:p.Lys101=
XM_005255233.5:c.303G>A	XP_005255290.1:p.Lys101=
XM_011545782.2:c.303G>A	XP_011544084.1:p.Lys101=
XM_024450221.1:c.909G>A	XP_024305989.1:p.Lys303=
NM_004960.4:c.918G>A MANE Select	NP_004951.1:p.Lys306=