Canonical Allele Identifier: CA395669934

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196371A>G (hg19) ; chr16:g.31185050A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185050A>G , CM000678.2:g.31185050A>G	GRCh38
NC_000016.9:g.31196371A>G , CM000678.1:g.31196371A>G	GRCh37
NC_000016.8:g.31103872A>G	NCBI36
NG_012889.2:g.9919A>G , LRG_655:g.9919A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.635A>G MANE Select	ENSP00000254108.8:p.Asp212Gly
ENST00000254108.11:c.635A>G	ENSP00000254108.7:p.Asp212Gly
ENST00000380244.7:c.632A>G	ENSP00000369594.3:p.Asp211Gly
ENST00000487509.6:n.700A>G
ENST00000566605.5:c.635A>G	ENSP00000455073.1:p.Asp212Gly
ENST00000568685.1:c.635A>G	ENSP00000455282.1:p.Asp212Gly
NM_001170634.1:c.632A>G	NP_001164105.1:p.Asp211Gly
NM_001170937.1:c.623A>G	NP_001164408.1:p.Asp208Gly
NM_004960.3:c.635A>G , LRG_655t1:c.635A>G	NP_004951.1:p.Asp212Gly
NR_028388.2:n.740A>G
XM_005255233.3:c.55A>G	XP_005255290.1:p.Thr19Ala
XM_011545781.1:c.629A>G	XP_011544083.1:p.Asp210Gly
XM_011545782.1:c.55A>G	XP_011544084.1:p.Thr19Ala
XM_005255233.5:c.55A>G	XP_005255290.1:p.Thr19Ala
XM_011545782.2:c.55A>G	XP_011544084.1:p.Thr19Ala
XM_024450221.1:c.626A>G	XP_024305989.1:p.Asp209Gly
NM_004960.4:c.635A>G MANE Select	NP_004951.1:p.Asp212Gly