Canonical Allele Identifier: CA395672430

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200525T>C (hg19) ; chr16:g.31189204T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189204T>C , CM000678.2:g.31189204T>C	GRCh38
NC_000016.9:g.31200525T>C , CM000678.1:g.31200525T>C	GRCh37
NC_000016.8:g.31108026T>C	NCBI36
NG_012889.2:g.14073T>C , LRG_655:g.14073T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.914T>C MANE Select	ENSP00000254108.8:p.Phe305Ser
ENST00000254108.11:c.914T>C	ENSP00000254108.7:p.Phe305Ser
ENST00000380244.7:c.911T>C	ENSP00000369594.3:p.Phe304Ser
ENST00000474990.5:n.208T>C
ENST00000487509.6:n.4089T>C
ENST00000564766.1:n.738T>C
ENST00000566605.5:c.*87T>C	ENSP00000455073.1:n.*87T>C
ENST00000568685.1:c.917T>C	ENSP00000455282.1:p.Phe306Ser
ENST00000568901.2:n.288T>C
NM_001170634.1:c.911T>C	NP_001164105.1:p.Phe304Ser
NM_001170937.1:c.902T>C	NP_001164408.1:p.Phe301Ser
NM_004960.3:c.914T>C , LRG_655t1:c.914T>C	NP_004951.1:p.Phe305Ser
NR_028388.2:n.984T>C
XM_005255233.3:c.299T>C	XP_005255290.1:p.Phe100Ser
XM_011545781.1:c.908T>C	XP_011544083.1:p.Phe303Ser
XM_011545782.1:c.299T>C	XP_011544084.1:p.Phe100Ser
XM_005255233.5:c.299T>C	XP_005255290.1:p.Phe100Ser
XM_011545782.2:c.299T>C	XP_011544084.1:p.Phe100Ser
XM_024450221.1:c.905T>C	XP_024305989.1:p.Phe302Ser
NM_004960.4:c.914T>C MANE Select	NP_004951.1:p.Phe305Ser