Canonical Allele Identifier: CA8023534

Gene: FUS

Linked Data

• dbSNP Id: rs765041157
• ExAC: 16:31195191 C / G
• gnomAD v2: 16-31195191-C-G
• MyVariant Identifiers: chr16:g.31195191C>G (hg19) ; chr16:g.31183870C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183870C>G , CM000678.2:g.31183870C>G	GRCh38
NC_000016.9:g.31195191C>G , CM000678.1:g.31195191C>G	GRCh37
NC_000016.8:g.31102692C>G	NCBI36
NG_012889.2:g.8739C>G , LRG_655:g.8739C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.203C>G MANE Select	ENSP00000254108.8:p.Thr68Ser
ENST00000254108.11:c.203C>G	ENSP00000254108.7:p.Thr68Ser
ENST00000380244.7:c.200C>G	ENSP00000369594.3:p.Thr67Ser
ENST00000487509.6:n.268C>G
ENST00000487974.1:n.321C>G
ENST00000566605.5:c.203C>G	ENSP00000455073.1:p.Thr68Ser
ENST00000568685.1:c.203C>G	ENSP00000455282.1:p.Thr68Ser
NM_001170634.1:c.200C>G	NP_001164105.1:p.Thr67Ser
NM_001170937.1:c.203C>G	NP_001164408.1:p.Thr68Ser
NM_004960.3:c.203C>G , LRG_655t1:c.203C>G	NP_004951.1:p.Thr68Ser
NR_028388.2:n.308C>G
XM_005255233.3:c.-378C>G	XP_005255290.1:n.-378C>G
XM_011545781.1:c.203C>G	XP_011544083.1:p.Thr68Ser
XM_005255233.5:c.-378C>G	XP_005255290.1:n.-378C>G
XM_024450221.1:c.200C>G	XP_024305989.1:p.Thr67Ser
NM_004960.4:c.203C>G MANE Select	NP_004951.1:p.Thr68Ser