Canonical Allele Identifier: CA395669830

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185023G>T , CM000678.2:g.31185023G>T	GRCh38
NC_000016.9:g.31196344G>T , CM000678.1:g.31196344G>T	GRCh37
NC_000016.8:g.31103845G>T	NCBI36
NG_012889.2:g.9892G>T , LRG_655:g.9892G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.608G>T MANE Select	NP_004951.1:p.Gly203Val
ENST00000254108.12:c.608G>T MANE Select	ENSP00000254108.8:p.Gly203Val
NM_001170634.1:c.605G>T	NP_001164105.1:p.Gly202Val
NM_001170937.1:c.596G>T	NP_001164408.1:p.Gly199Val
NM_004960.3:c.608G>T , LRG_655t1:c.608G>T	NP_004951.1:p.Gly203Val
NR_028388.2:n.713G>T
ENST00000254108.11:c.608G>T	ENSP00000254108.7:p.Gly203Val
ENST00000380244.7:c.605G>T	ENSP00000369594.3:p.Gly202Val
ENST00000487509.6:n.673G>T
ENST00000566605.5:c.608G>T	ENSP00000455073.1:p.Gly203Val
ENST00000568685.1:c.608G>T	ENSP00000455282.1:p.Gly203Val
XM_005255233.3:c.28G>T	XP_005255290.1:p.Val10Leu
XM_005255233.5:c.28G>T	XP_005255290.1:p.Val10Leu
XM_011545781.1:c.602G>T	XP_011544083.1:p.Gly201Val
XM_011545782.1:c.28G>T	XP_011544084.1:p.Val10Leu
XM_011545782.2:c.28G>T	XP_011544084.1:p.Val10Leu
XM_024450221.1:c.599G>T	XP_024305989.1:p.Gly200Val