Canonical Allele Identifier: CA8023625

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184325C>T , CM000678.2:g.31184325C>T	GRCh38
NC_000016.9:g.31195646C>T , CM000678.1:g.31195646C>T	GRCh37
NC_000016.8:g.31103147C>T	NCBI36
NG_012889.2:g.9194C>T , LRG_655:g.9194C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.452C>T MANE Select	NP_004951.1:p.Pro151Leu
ENST00000254108.12:c.452C>T MANE Select	ENSP00000254108.8:p.Pro151Leu
NM_001170634.1:c.449C>T	NP_001164105.1:p.Pro150Leu
NM_001170937.1:c.452C>T	NP_001164408.1:p.Pro151Leu
NM_004960.3:c.452C>T , LRG_655t1:c.452C>T	NP_004951.1:p.Pro151Leu
NR_028388.2:n.557C>T
ENST00000254108.11:c.452C>T	ENSP00000254108.7:p.Pro151Leu
ENST00000380244.7:c.449C>T	ENSP00000369594.3:p.Pro150Leu
ENST00000487509.6:n.517C>T
ENST00000487974.1:n.570C>T
ENST00000566605.5:c.452C>T	ENSP00000455073.1:p.Pro151Leu
ENST00000568685.1:c.452C>T	ENSP00000455282.1:p.Pro151Leu
XM_005255233.3:c.-129C>T	XP_005255290.1:n.-129C>T
XM_005255233.5:c.-129C>T	XP_005255290.1:n.-129C>T
XM_011545781.1:c.452C>T	XP_011544083.1:p.Pro151Leu
XM_011545782.1:c.-123C>T	XP_011544084.1:n.-123C>T
XM_024450221.1:c.449C>T	XP_024305989.1:p.Pro150Leu