Canonical Allele Identifier: CA395667004

Gene: FUS

Linked Data

• COSMIC: COSM6311223 ; COSM6311224
• MyVariant Identifiers: chr16:g.31195290G>T (hg19) ; chr16:g.31183969G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183969G>T , CM000678.2:g.31183969G>T	GRCh38
NC_000016.9:g.31195290G>T , CM000678.1:g.31195290G>T	GRCh37
NC_000016.8:g.31102791G>T	NCBI36
NG_012889.2:g.8838G>T , LRG_655:g.8838G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.302G>T MANE Select	ENSP00000254108.8:p.Gly101Val
ENST00000254108.11:c.302G>T	ENSP00000254108.7:p.Gly101Val
ENST00000380244.7:c.299G>T	ENSP00000369594.3:p.Gly100Val
ENST00000487509.6:n.367G>T
ENST00000487974.1:n.420G>T
ENST00000566605.5:c.302G>T	ENSP00000455073.1:p.Gly101Val
ENST00000568685.1:c.302G>T	ENSP00000455282.1:p.Gly101Val
NM_001170634.1:c.299G>T	NP_001164105.1:p.Gly100Val
NM_001170937.1:c.302G>T	NP_001164408.1:p.Gly101Val
NM_004960.3:c.302G>T , LRG_655t1:c.302G>T	NP_004951.1:p.Gly101Val
NR_028388.2:n.407G>T
XM_005255233.3:c.-279G>T	XP_005255290.1:n.-279G>T
XM_011545781.1:c.302G>T	XP_011544083.1:p.Gly101Val
XM_005255233.5:c.-279G>T	XP_005255290.1:n.-279G>T
XM_024450221.1:c.299G>T	XP_024305989.1:p.Gly100Val
NM_004960.4:c.302G>T MANE Select	NP_004951.1:p.Gly101Val