Canonical Allele Identifier: CA494713698

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200514G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189193G>T , CM000678.2:g.31189193G>T	GRCh38
NC_000016.9:g.31200514G>T , CM000678.1:g.31200514G>T	GRCh37
NC_000016.8:g.31108015G>T	NCBI36
NG_012889.2:g.14062G>T , LRG_655:g.14062G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.903G>T MANE Select	ENSP00000254108.8:p.Val301=
ENST00000254108.11:c.903G>T	ENSP00000254108.7:p.Val301=
ENST00000380244.7:c.900G>T	ENSP00000369594.3:p.Val300=
ENST00000474990.5:n.197G>T
ENST00000487509.6:n.4078G>T
ENST00000564766.1:n.727G>T
ENST00000566605.5:c.*76G>T	ENSP00000455073.1:n.*76G>T
ENST00000568685.1:c.906G>T	ENSP00000455282.1:p.Val302=
ENST00000568901.2:n.277G>T
NM_001170634.1:c.900G>T	NP_001164105.1:p.Val300=
NM_001170937.1:c.891G>T	NP_001164408.1:p.Val297=
NM_004960.3:c.903G>T , LRG_655t1:c.903G>T	NP_004951.1:p.Val301=
NR_028388.2:n.973G>T
XM_005255233.3:c.288G>T	XP_005255290.1:p.Val96=
XM_011545781.1:c.897G>T	XP_011544083.1:p.Val299=
XM_011545782.1:c.288G>T	XP_011544084.1:p.Val96=
XM_005255233.5:c.288G>T	XP_005255290.1:p.Val96=
XM_011545782.2:c.288G>T	XP_011544084.1:p.Val96=
XM_024450221.1:c.894G>T	XP_024305989.1:p.Val298=
NM_004960.4:c.903G>T MANE Select	NP_004951.1:p.Val301=