Canonical Allele Identifier: CA395672180

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200488G>C (hg19) ; chr16:g.31189167G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189167G>C , CM000678.2:g.31189167G>C	GRCh38
NC_000016.9:g.31200488G>C , CM000678.1:g.31200488G>C	GRCh37
NC_000016.8:g.31107989G>C	NCBI36
NG_012889.2:g.14036G>C , LRG_655:g.14036G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.877G>C MANE Select	ENSP00000254108.8:p.Gly293Arg
ENST00000254108.11:c.877G>C	ENSP00000254108.7:p.Gly293Arg
ENST00000380244.7:c.874G>C	ENSP00000369594.3:p.Gly292Arg
ENST00000474990.5:n.171G>C
ENST00000487509.6:n.4052G>C
ENST00000564766.1:n.701G>C
ENST00000566605.5:c.*50G>C	ENSP00000455073.1:n.*50G>C
ENST00000568685.1:c.880G>C	ENSP00000455282.1:p.Gly294Arg
ENST00000568901.2:n.251G>C
NM_001170634.1:c.874G>C	NP_001164105.1:p.Gly292Arg
NM_001170937.1:c.865G>C	NP_001164408.1:p.Gly289Arg
NM_004960.3:c.877G>C , LRG_655t1:c.877G>C	NP_004951.1:p.Gly293Arg
NR_028388.2:n.947G>C
XM_005255233.3:c.262G>C	XP_005255290.1:p.Gly88Arg
XM_011545781.1:c.871G>C	XP_011544083.1:p.Gly291Arg
XM_011545782.1:c.262G>C	XP_011544084.1:p.Gly88Arg
XM_005255233.5:c.262G>C	XP_005255290.1:p.Gly88Arg
XM_011545782.2:c.262G>C	XP_011544084.1:p.Gly88Arg
XM_024450221.1:c.868G>C	XP_024305989.1:p.Gly290Arg
NM_004960.4:c.877G>C MANE Select	NP_004951.1:p.Gly293Arg