Canonical Allele Identifier: CA8024024

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31190797C>T , CM000678.2:g.31190797C>T	GRCh38
NC_000016.9:g.31202118C>T , CM000678.1:g.31202118C>T	GRCh37
NC_000016.8:g.31109619C>T	NCBI36
NG_012889.2:g.15666C>T , LRG_655:g.15666C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1348C>T MANE Select	NP_004951.1:p.Pro450Ser
ENST00000254108.12:c.1348C>T MANE Select	ENSP00000254108.8:p.Pro450Ser
NM_001170634.1:c.1345C>T	NP_001164105.1:p.Pro449Ser
NM_001170937.1:c.1336C>T	NP_001164408.1:p.Pro446Ser
NM_004960.3:c.1348C>T , LRG_655t1:c.1348C>T	NP_004951.1:p.Pro450Ser
NR_028388.2:n.1418C>T
ENST00000254108.11:c.1348C>T	ENSP00000254108.7:p.Pro450Ser
ENST00000380244.7:c.1345C>T	ENSP00000369594.3:p.Pro449Ser
ENST00000474990.5:n.642C>T
ENST00000483853.1:n.425C>T
ENST00000487509.6:n.4523C>T
ENST00000566605.5:c.*521C>T	ENSP00000455073.1:n.*521C>T
ENST00000568685.1:c.1351C>T	ENSP00000455282.1:p.Pro451Ser
ENST00000569760.5:n.239C>T
XM_005255233.3:c.733C>T	XP_005255290.1:p.Pro245Ser
XM_005255233.5:c.733C>T	XP_005255290.1:p.Pro245Ser
XM_011545781.1:c.1342C>T	XP_011544083.1:p.Pro448Ser
XM_011545782.1:c.733C>T	XP_011544084.1:p.Pro245Ser
XM_011545782.2:c.733C>T	XP_011544084.1:p.Pro245Ser
XM_024450221.1:c.1339C>T	XP_024305989.1:p.Pro447Ser