Canonical Allele Identifier: CA494713676

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200499T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189178T>G , CM000678.2:g.31189178T>G	GRCh38
NC_000016.9:g.31200499T>G , CM000678.1:g.31200499T>G	GRCh37
NC_000016.8:g.31108000T>G	NCBI36
NG_012889.2:g.14047T>G , LRG_655:g.14047T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.888T>G MANE Select	ENSP00000254108.8:p.Val296=
ENST00000254108.11:c.888T>G	ENSP00000254108.7:p.Val296=
ENST00000380244.7:c.885T>G	ENSP00000369594.3:p.Val295=
ENST00000474990.5:n.182T>G
ENST00000487509.6:n.4063T>G
ENST00000564766.1:n.712T>G
ENST00000566605.5:c.*61T>G	ENSP00000455073.1:n.*61T>G
ENST00000568685.1:c.891T>G	ENSP00000455282.1:p.Val297=
ENST00000568901.2:n.262T>G
NM_001170634.1:c.885T>G	NP_001164105.1:p.Val295=
NM_001170937.1:c.876T>G	NP_001164408.1:p.Val292=
NM_004960.3:c.888T>G , LRG_655t1:c.888T>G	NP_004951.1:p.Val296=
NR_028388.2:n.958T>G
XM_005255233.3:c.273T>G	XP_005255290.1:p.Val91=
XM_011545781.1:c.882T>G	XP_011544083.1:p.Val294=
XM_011545782.1:c.273T>G	XP_011544084.1:p.Val91=
XM_005255233.5:c.273T>G	XP_005255290.1:p.Val91=
XM_011545782.2:c.273T>G	XP_011544084.1:p.Val91=
XM_024450221.1:c.879T>G	XP_024305989.1:p.Val293=
NM_004960.4:c.888T>G MANE Select	NP_004951.1:p.Val296=