Canonical Allele Identifier: CA395666420

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31195190A>C (hg19) ; chr16:g.31183869A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31183869A>C , CM000678.2:g.31183869A>C	GRCh38
NC_000016.9:g.31195190A>C , CM000678.1:g.31195190A>C	GRCh37
NC_000016.8:g.31102691A>C	NCBI36
NG_012889.2:g.8738A>C , LRG_655:g.8738A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.202A>C MANE Select	ENSP00000254108.8:p.Thr68Pro
ENST00000254108.11:c.202A>C	ENSP00000254108.7:p.Thr68Pro
ENST00000380244.7:c.199A>C	ENSP00000369594.3:p.Thr67Pro
ENST00000487509.6:n.267A>C
ENST00000487974.1:n.320A>C
ENST00000566605.5:c.202A>C	ENSP00000455073.1:p.Thr68Pro
ENST00000568685.1:c.202A>C	ENSP00000455282.1:p.Thr68Pro
NM_001170634.1:c.199A>C	NP_001164105.1:p.Thr67Pro
NM_001170937.1:c.202A>C	NP_001164408.1:p.Thr68Pro
NM_004960.3:c.202A>C , LRG_655t1:c.202A>C	NP_004951.1:p.Thr68Pro
NR_028388.2:n.307A>C
XM_005255233.3:c.-379A>C	XP_005255290.1:n.-379A>C
XM_011545781.1:c.202A>C	XP_011544083.1:p.Thr68Pro
XM_005255233.5:c.-379A>C	XP_005255290.1:n.-379A>C
XM_024450221.1:c.199A>C	XP_024305989.1:p.Thr67Pro
NM_004960.4:c.202A>C MANE Select	NP_004951.1:p.Thr68Pro