Canonical Allele Identifier: CA395675108

Gene: FUS

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31190398C>A , CM000678.2:g.31190398C>A	GRCh38
NC_000016.9:g.31201719C>A , CM000678.1:g.31201719C>A	GRCh37
NC_000016.8:g.31109220C>A	NCBI36
NG_012889.2:g.15267C>A , LRG_655:g.15267C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.1292C>A MANE Select	ENSP00000254108.8:p.Pro431His
ENST00000254108.11:c.1292C>A	ENSP00000254108.7:p.Pro431His
ENST00000380244.7:c.1289C>A	ENSP00000369594.3:p.Pro430His
ENST00000474990.5:n.586C>A
ENST00000483853.1:n.26C>A
ENST00000487509.6:n.4467C>A
ENST00000566605.5:c.*465C>A	ENSP00000455073.1:n.*465C>A
ENST00000568685.1:c.1295C>A	ENSP00000455282.1:p.Pro432His
ENST00000569760.5:n.183C>A
NM_001170634.1:c.1289C>A	NP_001164105.1:p.Pro430His
NM_001170937.1:c.1280C>A	NP_001164408.1:p.Pro427His
NM_004960.3:c.1292C>A , LRG_655t1:c.1292C>A	NP_004951.1:p.Pro431His
NR_028388.2:n.1362C>A
XM_005255233.3:c.677C>A	XP_005255290.1:p.Pro226His
XM_011545781.1:c.1286C>A	XP_011544083.1:p.Pro429His
XM_011545782.1:c.677C>A	XP_011544084.1:p.Pro226His
XM_005255233.5:c.677C>A	XP_005255290.1:p.Pro226His
XM_011545782.2:c.677C>A	XP_011544084.1:p.Pro226His
XM_024450221.1:c.1283C>A	XP_024305989.1:p.Pro428His
NM_004960.4:c.1292C>A MANE Select	NP_004951.1:p.Pro431His