Canonical Allele Identifier: CA395672120

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200479C>A (hg19) ; chr16:g.31189158C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189158C>A , CM000678.2:g.31189158C>A	GRCh38
NC_000016.9:g.31200479C>A , CM000678.1:g.31200479C>A	GRCh37
NC_000016.8:g.31107980C>A	NCBI36
NG_012889.2:g.14027C>A , LRG_655:g.14027C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000254108.12:c.868C>A MANE Select	ENSP00000254108.8:p.Gln290Lys
ENST00000254108.11:c.868C>A	ENSP00000254108.7:p.Gln290Lys
ENST00000380244.7:c.865C>A	ENSP00000369594.3:p.Gln289Lys
ENST00000474990.5:n.162C>A
ENST00000487509.6:n.4043C>A
ENST00000564766.1:n.692C>A
ENST00000566605.5:c.*41C>A	ENSP00000455073.1:n.*41C>A
ENST00000568685.1:c.871C>A	ENSP00000455282.1:p.Gln291Lys
ENST00000568901.2:n.242C>A
NM_001170634.1:c.865C>A	NP_001164105.1:p.Gln289Lys
NM_001170937.1:c.856C>A	NP_001164408.1:p.Gln286Lys
NM_004960.3:c.868C>A , LRG_655t1:c.868C>A	NP_004951.1:p.Gln290Lys
NR_028388.2:n.938C>A
XM_005255233.3:c.253C>A	XP_005255290.1:p.Gln85Lys
XM_011545781.1:c.862C>A	XP_011544083.1:p.Gln288Lys
XM_011545782.1:c.253C>A	XP_011544084.1:p.Gln85Lys
XM_005255233.5:c.253C>A	XP_005255290.1:p.Gln85Lys
XM_011545782.2:c.253C>A	XP_011544084.1:p.Gln85Lys
XM_024450221.1:c.859C>A	XP_024305989.1:p.Gln287Lys
NM_004960.4:c.868C>A MANE Select	NP_004951.1:p.Gln290Lys