Canonical Allele Identifier: CA395672168

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200486T>C (hg19) ; chr16:g.31189165T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189165T>C , CM000678.2:g.31189165T>C	GRCh38
NC_000016.9:g.31200486T>C , CM000678.1:g.31200486T>C	GRCh37
NC_000016.8:g.31107987T>C	NCBI36
NG_012889.2:g.14034T>C , LRG_655:g.14034T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.875T>C MANE Select	ENSP00000254108.8:p.Leu292Pro
ENST00000254108.11:c.875T>C	ENSP00000254108.7:p.Leu292Pro
ENST00000380244.7:c.872T>C	ENSP00000369594.3:p.Leu291Pro
ENST00000474990.5:n.169T>C
ENST00000487509.6:n.4050T>C
ENST00000564766.1:n.699T>C
ENST00000566605.5:c.*48T>C	ENSP00000455073.1:n.*48T>C
ENST00000568685.1:c.878T>C	ENSP00000455282.1:p.Leu293Pro
ENST00000568901.2:n.249T>C
NM_001170634.1:c.872T>C	NP_001164105.1:p.Leu291Pro
NM_001170937.1:c.863T>C	NP_001164408.1:p.Leu288Pro
NM_004960.3:c.875T>C , LRG_655t1:c.875T>C	NP_004951.1:p.Leu292Pro
NR_028388.2:n.945T>C
XM_005255233.3:c.260T>C	XP_005255290.1:p.Leu87Pro
XM_011545781.1:c.869T>C	XP_011544083.1:p.Leu290Pro
XM_011545782.1:c.260T>C	XP_011544084.1:p.Leu87Pro
XM_005255233.5:c.260T>C	XP_005255290.1:p.Leu87Pro
XM_011545782.2:c.260T>C	XP_011544084.1:p.Leu87Pro
XM_024450221.1:c.866T>C	XP_024305989.1:p.Leu289Pro
NM_004960.4:c.875T>C MANE Select	NP_004951.1:p.Leu292Pro