Canonical Allele Identifier: CA395672047

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200463C>A (hg19) ; chr16:g.31189142C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189142C>A , CM000678.2:g.31189142C>A	GRCh38
NC_000016.9:g.31200463C>A , CM000678.1:g.31200463C>A	GRCh37
NC_000016.8:g.31107964C>A	NCBI36
NG_012889.2:g.14011C>A , LRG_655:g.14011C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.852C>A MANE Select	ENSP00000254108.8:p.Asn284Lys
ENST00000254108.11:c.852C>A	ENSP00000254108.7:p.Asn284Lys
ENST00000380244.7:c.849C>A	ENSP00000369594.3:p.Asn283Lys
ENST00000474990.5:n.146C>A
ENST00000487509.6:n.4027C>A
ENST00000564766.1:n.676C>A
ENST00000566605.5:c.*25C>A	ENSP00000455073.1:n.*25C>A
ENST00000568685.1:c.855C>A	ENSP00000455282.1:p.Asn285Lys
ENST00000568901.2:n.226C>A
NM_001170634.1:c.849C>A	NP_001164105.1:p.Asn283Lys
NM_001170937.1:c.840C>A	NP_001164408.1:p.Asn280Lys
NM_004960.3:c.852C>A , LRG_655t1:c.852C>A	NP_004951.1:p.Asn284Lys
NR_028388.2:n.922C>A
XM_005255233.3:c.237C>A	XP_005255290.1:p.Asn79Lys
XM_011545781.1:c.846C>A	XP_011544083.1:p.Asn282Lys
XM_011545782.1:c.237C>A	XP_011544084.1:p.Asn79Lys
XM_005255233.5:c.237C>A	XP_005255290.1:p.Asn79Lys
XM_011545782.2:c.237C>A	XP_011544084.1:p.Asn79Lys
XM_024450221.1:c.843C>A	XP_024305989.1:p.Asn281Lys
NM_004960.4:c.852C>A MANE Select	NP_004951.1:p.Asn284Lys