Canonical Allele Identifier: CA8023668

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184438C>T , CM000678.2:g.31184438C>T	GRCh38
NC_000016.9:g.31195759C>T , CM000678.1:g.31195759C>T	GRCh37
NC_000016.8:g.31103260C>T	NCBI36
NG_012889.2:g.9307C>T , LRG_655:g.9307C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.523+42C>T MANE Select	ENSP00000254108.8:n.523+42C>T
ENST00000254108.11:c.523+42C>T	ENSP00000254108.7:n.523+42C>T
ENST00000380244.7:c.520+42C>T	ENSP00000369594.3:n.520+42C>T
ENST00000487509.6:n.588+42C>T
ENST00000566605.5:c.523+42C>T	ENSP00000455073.1:n.523+42C>T
ENST00000568685.1:c.523+42C>T	ENSP00000455282.1:n.523+42C>T
NM_001170634.1:c.520+42C>T	NP_001164105.1:n.520+42C>T
NM_001170937.1:c.511+54C>T	NP_001164408.1:n.511+54C>T
NM_004960.3:c.523+42C>T , LRG_655t1:c.523+42C>T	NP_004951.1:n.523+42C>T
NR_028388.2:n.628+42C>T
XM_005255233.3:c.-58+42C>T	XP_005255290.1:n.-58+42C>T
XM_011545781.1:c.517+48C>T	XP_011544083.1:n.517+48C>T
XM_011545782.1:c.-58+48C>T	XP_011544084.1:n.-58+48C>T
XM_005255233.5:c.-58+42C>T	XP_005255290.1:n.-58+42C>T
XM_011545782.2:c.-58+48C>T	XP_011544084.1:n.-58+48C>T
XM_024450221.1:c.514+48C>T	XP_024305989.1:n.514+48C>T
NM_004960.4:c.523+42C>T MANE Select	NP_004951.1:n.523+42C>T