Canonical Allele Identifier: CA8024054

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31190965G>A , CM000678.2:g.31190965G>A	GRCh38
NC_000016.9:g.31202286G>A , CM000678.1:g.31202286G>A	GRCh37
NC_000016.8:g.31109787G>A	NCBI36
NG_012889.2:g.15834G>A , LRG_655:g.15834G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.1396G>A MANE Select	NP_004951.1:p.Gly466Ser
ENST00000254108.12:c.1396G>A MANE Select	ENSP00000254108.8:p.Gly466Ser
NM_001170634.1:c.1393G>A	NP_001164105.1:p.Gly465Ser
NM_001170937.1:c.1384G>A	NP_001164408.1:p.Gly462Ser
NM_004960.3:c.1396G>A , LRG_655t1:c.1396G>A	NP_004951.1:p.Gly466Ser
NR_028388.2:n.1466G>A
ENST00000254108.11:c.1396G>A	ENSP00000254108.7:p.Gly466Ser
ENST00000380244.7:c.1393G>A	ENSP00000369594.3:p.Gly465Ser
ENST00000474990.5:n.690G>A
ENST00000483853.1:n.473G>A
ENST00000487509.6:n.4571G>A
ENST00000566605.5:c.*569G>A	ENSP00000455073.1:n.*569G>A
ENST00000568685.1:c.1399G>A	ENSP00000455282.1:p.Gly467Ser
ENST00000569760.5:n.287G>A
XM_005255233.3:c.781G>A	XP_005255290.1:p.Gly261Ser
XM_005255233.5:c.781G>A	XP_005255290.1:p.Gly261Ser
XM_011545781.1:c.1390G>A	XP_011544083.1:p.Gly464Ser
XM_011545782.1:c.781G>A	XP_011544084.1:p.Gly261Ser
XM_011545782.2:c.781G>A	XP_011544084.1:p.Gly261Ser
XM_024450221.1:c.1387G>A	XP_024305989.1:p.Gly463Ser