Canonical Allele Identifier: CA395672097

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200474T>C (hg19) ; chr16:g.31189153T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189153T>C , CM000678.2:g.31189153T>C	GRCh38
NC_000016.9:g.31200474T>C , CM000678.1:g.31200474T>C	GRCh37
NC_000016.8:g.31107975T>C	NCBI36
NG_012889.2:g.14022T>C , LRG_655:g.14022T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.863T>C MANE Select	ENSP00000254108.8:p.Phe288Ser
ENST00000254108.11:c.863T>C	ENSP00000254108.7:p.Phe288Ser
ENST00000380244.7:c.860T>C	ENSP00000369594.3:p.Phe287Ser
ENST00000474990.5:n.157T>C
ENST00000487509.6:n.4038T>C
ENST00000564766.1:n.687T>C
ENST00000566605.5:c.*36T>C	ENSP00000455073.1:n.*36T>C
ENST00000568685.1:c.866T>C	ENSP00000455282.1:p.Phe289Ser
ENST00000568901.2:n.237T>C
NM_001170634.1:c.860T>C	NP_001164105.1:p.Phe287Ser
NM_001170937.1:c.851T>C	NP_001164408.1:p.Phe284Ser
NM_004960.3:c.863T>C , LRG_655t1:c.863T>C	NP_004951.1:p.Phe288Ser
NR_028388.2:n.933T>C
XM_005255233.3:c.248T>C	XP_005255290.1:p.Phe83Ser
XM_011545781.1:c.857T>C	XP_011544083.1:p.Phe286Ser
XM_011545782.1:c.248T>C	XP_011544084.1:p.Phe83Ser
XM_005255233.5:c.248T>C	XP_005255290.1:p.Phe83Ser
XM_011545782.2:c.248T>C	XP_011544084.1:p.Phe83Ser
XM_024450221.1:c.854T>C	XP_024305989.1:p.Phe285Ser
NM_004960.4:c.863T>C MANE Select	NP_004951.1:p.Phe288Ser