Canonical Allele Identifier: CA395669895

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196364C>A (hg19) ; chr16:g.31185043C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185043C>A , CM000678.2:g.31185043C>A	GRCh38
NC_000016.9:g.31196364C>A , CM000678.1:g.31196364C>A	GRCh37
NC_000016.8:g.31103865C>A	NCBI36
NG_012889.2:g.9912C>A , LRG_655:g.9912C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.628C>A MANE Select	ENSP00000254108.8:p.Gln210Lys
ENST00000254108.11:c.628C>A	ENSP00000254108.7:p.Gln210Lys
ENST00000380244.7:c.625C>A	ENSP00000369594.3:p.Gln209Lys
ENST00000487509.6:n.693C>A
ENST00000566605.5:c.628C>A	ENSP00000455073.1:p.Gln210Lys
ENST00000568685.1:c.628C>A	ENSP00000455282.1:p.Gln210Lys
NM_001170634.1:c.625C>A	NP_001164105.1:p.Gln209Lys
NM_001170937.1:c.616C>A	NP_001164408.1:p.Gln206Lys
NM_004960.3:c.628C>A , LRG_655t1:c.628C>A	NP_004951.1:p.Gln210Lys
NR_028388.2:n.733C>A
XM_005255233.3:c.48C>A	XP_005255290.1:p.Asp16Glu
XM_011545781.1:c.622C>A	XP_011544083.1:p.Gln208Lys
XM_011545782.1:c.48C>A	XP_011544084.1:p.Asp16Glu
XM_005255233.5:c.48C>A	XP_005255290.1:p.Asp16Glu
XM_011545782.2:c.48C>A	XP_011544084.1:p.Asp16Glu
XM_024450221.1:c.619C>A	XP_024305989.1:p.Gln207Lys
NM_004960.4:c.628C>A MANE Select	NP_004951.1:p.Gln210Lys