Canonical Allele Identifier: CA395666968

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31195284G>C (hg19) ; chr16:g.31183963G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183963G>C , CM000678.2:g.31183963G>C	GRCh38
NC_000016.9:g.31195284G>C , CM000678.1:g.31195284G>C	GRCh37
NC_000016.8:g.31102785G>C	NCBI36
NG_012889.2:g.8832G>C , LRG_655:g.8832G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.296G>C MANE Select	ENSP00000254108.8:p.Gly99Ala
ENST00000254108.11:c.296G>C	ENSP00000254108.7:p.Gly99Ala
ENST00000380244.7:c.293G>C	ENSP00000369594.3:p.Gly98Ala
ENST00000487509.6:n.361G>C
ENST00000487974.1:n.414G>C
ENST00000566605.5:c.296G>C	ENSP00000455073.1:p.Gly99Ala
ENST00000568685.1:c.296G>C	ENSP00000455282.1:p.Gly99Ala
NM_001170634.1:c.293G>C	NP_001164105.1:p.Gly98Ala
NM_001170937.1:c.296G>C	NP_001164408.1:p.Gly99Ala
NM_004960.3:c.296G>C , LRG_655t1:c.296G>C	NP_004951.1:p.Gly99Ala
NR_028388.2:n.401G>C
XM_005255233.3:c.-285G>C	XP_005255290.1:n.-285G>C
XM_011545781.1:c.296G>C	XP_011544083.1:p.Gly99Ala
XM_005255233.5:c.-285G>C	XP_005255290.1:n.-285G>C
XM_024450221.1:c.293G>C	XP_024305989.1:p.Gly98Ala
NM_004960.4:c.296G>C MANE Select	NP_004951.1:p.Gly99Ala