Canonical Allele Identifier: CA395669470

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196260G>T (hg19) ; chr16:g.31184939G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184939G>T , CM000678.2:g.31184939G>T	GRCh38
NC_000016.9:g.31196260G>T , CM000678.1:g.31196260G>T	GRCh37
NC_000016.8:g.31103761G>T	NCBI36
NG_012889.2:g.9808G>T , LRG_655:g.9808G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524G>T MANE Select	ENSP00000254108.8:p.Gly175Val
ENST00000254108.11:c.524G>T	ENSP00000254108.7:p.Gly175Val
ENST00000380244.7:c.521G>T	ENSP00000369594.3:p.Gly174Val
ENST00000487509.6:n.589G>T
ENST00000566605.5:c.524G>T	ENSP00000455073.1:p.Gly175Val
ENST00000568685.1:c.524G>T	ENSP00000455282.1:p.Gly175Val
NM_001170634.1:c.521G>T	NP_001164105.1:p.Gly174Val
NM_001170937.1:c.512G>T	NP_001164408.1:p.Gly171Val
NM_004960.3:c.524G>T , LRG_655t1:c.524G>T	NP_004951.1:p.Gly175Val
NR_028388.2:n.629G>T
XM_005255233.3:c.-57G>T	XP_005255290.1:n.-57G>T
XM_011545781.1:c.518G>T	XP_011544083.1:p.Gly173Val
XM_011545782.1:c.-57G>T	XP_011544084.1:n.-57G>T
XM_005255233.5:c.-57G>T	XP_005255290.1:n.-57G>T
XM_011545782.2:c.-57G>T	XP_011544084.1:n.-57G>T
XM_024450221.1:c.515G>T	XP_024305989.1:p.Gly172Val
NM_004960.4:c.524G>T MANE Select	NP_004951.1:p.Gly175Val