Canonical Allele Identifier: CA395669564

Gene: FUS

Linked Data

• gnomAD v4: 16-31184955-T-G
• MyVariant Identifiers: chr16:g.31196276T>G (hg19) ; chr16:g.31184955T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184955T>G , CM000678.2:g.31184955T>G	GRCh38
NC_000016.9:g.31196276T>G , CM000678.1:g.31196276T>G	GRCh37
NC_000016.8:g.31103777T>G	NCBI36
NG_012889.2:g.9824T>G , LRG_655:g.9824T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.540T>G MANE Select	ENSP00000254108.8:p.Asp180Glu
ENST00000254108.11:c.540T>G	ENSP00000254108.7:p.Asp180Glu
ENST00000380244.7:c.537T>G	ENSP00000369594.3:p.Asp179Glu
ENST00000487509.6:n.605T>G
ENST00000566605.5:c.540T>G	ENSP00000455073.1:p.Asp180Glu
ENST00000568685.1:c.540T>G	ENSP00000455282.1:p.Asp180Glu
NM_001170634.1:c.537T>G	NP_001164105.1:p.Asp179Glu
NM_001170937.1:c.528T>G	NP_001164408.1:p.Asp176Glu
NM_004960.3:c.540T>G , LRG_655t1:c.540T>G	NP_004951.1:p.Asp180Glu
NR_028388.2:n.645T>G
XM_005255233.3:c.-41T>G	XP_005255290.1:n.-41T>G
XM_011545781.1:c.534T>G	XP_011544083.1:p.Asp178Glu
XM_011545782.1:c.-41T>G	XP_011544084.1:n.-41T>G
XM_005255233.5:c.-41T>G	XP_005255290.1:n.-41T>G
XM_011545782.2:c.-41T>G	XP_011544084.1:n.-41T>G
XM_024450221.1:c.531T>G	XP_024305989.1:p.Asp177Glu
NM_004960.4:c.540T>G MANE Select	NP_004951.1:p.Asp180Glu