Canonical Allele Identifier: CA395672055

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200465A>G (hg19) ; chr16:g.31189144A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189144A>G , CM000678.2:g.31189144A>G	GRCh38
NC_000016.9:g.31200465A>G , CM000678.1:g.31200465A>G	GRCh37
NC_000016.8:g.31107966A>G	NCBI36
NG_012889.2:g.14013A>G , LRG_655:g.14013A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.854A>G MANE Select	ENSP00000254108.8:p.Asn285Ser
ENST00000254108.11:c.854A>G	ENSP00000254108.7:p.Asn285Ser
ENST00000380244.7:c.851A>G	ENSP00000369594.3:p.Asn284Ser
ENST00000474990.5:n.148A>G
ENST00000487509.6:n.4029A>G
ENST00000564766.1:n.678A>G
ENST00000566605.5:c.*27A>G	ENSP00000455073.1:n.*27A>G
ENST00000568685.1:c.857A>G	ENSP00000455282.1:p.Asn286Ser
ENST00000568901.2:n.228A>G
NM_001170634.1:c.851A>G	NP_001164105.1:p.Asn284Ser
NM_001170937.1:c.842A>G	NP_001164408.1:p.Asn281Ser
NM_004960.3:c.854A>G , LRG_655t1:c.854A>G	NP_004951.1:p.Asn285Ser
NR_028388.2:n.924A>G
XM_005255233.3:c.239A>G	XP_005255290.1:p.Asn80Ser
XM_011545781.1:c.848A>G	XP_011544083.1:p.Asn283Ser
XM_011545782.1:c.239A>G	XP_011544084.1:p.Asn80Ser
XM_005255233.5:c.239A>G	XP_005255290.1:p.Asn80Ser
XM_011545782.2:c.239A>G	XP_011544084.1:p.Asn80Ser
XM_024450221.1:c.845A>G	XP_024305989.1:p.Asn282Ser
NM_004960.4:c.854A>G MANE Select	NP_004951.1:p.Asn285Ser