Canonical Allele Identifier: CA494713653

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200484C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189163C>G , CM000678.2:g.31189163C>G	GRCh38
NC_000016.9:g.31200484C>G , CM000678.1:g.31200484C>G	GRCh37
NC_000016.8:g.31107985C>G	NCBI36
NG_012889.2:g.14032C>G , LRG_655:g.14032C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.873C>G MANE Select	ENSP00000254108.8:p.Gly291=
ENST00000254108.11:c.873C>G	ENSP00000254108.7:p.Gly291=
ENST00000380244.7:c.870C>G	ENSP00000369594.3:p.Gly290=
ENST00000474990.5:n.167C>G
ENST00000487509.6:n.4048C>G
ENST00000564766.1:n.697C>G
ENST00000566605.5:c.*46C>G	ENSP00000455073.1:n.*46C>G
ENST00000568685.1:c.876C>G	ENSP00000455282.1:p.Gly292=
ENST00000568901.2:n.247C>G
NM_001170634.1:c.870C>G	NP_001164105.1:p.Gly290=
NM_001170937.1:c.861C>G	NP_001164408.1:p.Gly287=
NM_004960.3:c.873C>G , LRG_655t1:c.873C>G	NP_004951.1:p.Gly291=
NR_028388.2:n.943C>G
XM_005255233.3:c.258C>G	XP_005255290.1:p.Gly86=
XM_011545781.1:c.867C>G	XP_011544083.1:p.Gly289=
XM_011545782.1:c.258C>G	XP_011544084.1:p.Gly86=
XM_005255233.5:c.258C>G	XP_005255290.1:p.Gly86=
XM_011545782.2:c.258C>G	XP_011544084.1:p.Gly86=
XM_024450221.1:c.864C>G	XP_024305989.1:p.Gly288=
NM_004960.4:c.873C>G MANE Select	NP_004951.1:p.Gly291=