Canonical Allele Identifier: CA494928730

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31196345T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185024T>A , CM000678.2:g.31185024T>A	GRCh38
NC_000016.9:g.31196345T>A , CM000678.1:g.31196345T>A	GRCh37
NC_000016.8:g.31103846T>A	NCBI36
NG_012889.2:g.9893T>A , LRG_655:g.9893T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.609T>A MANE Select	ENSP00000254108.8:p.Gly203=
ENST00000254108.11:c.609T>A	ENSP00000254108.7:p.Gly203=
ENST00000380244.7:c.606T>A	ENSP00000369594.3:p.Gly202=
ENST00000487509.6:n.674T>A
ENST00000566605.5:c.609T>A	ENSP00000455073.1:p.Gly203=
ENST00000568685.1:c.609T>A	ENSP00000455282.1:p.Gly203=
NM_001170634.1:c.606T>A	NP_001164105.1:p.Gly202=
NM_001170937.1:c.597T>A	NP_001164408.1:p.Gly199=
NM_004960.3:c.609T>A , LRG_655t1:c.609T>A	NP_004951.1:p.Gly203=
NR_028388.2:n.714T>A
XM_005255233.3:c.29T>A	XP_005255290.1:p.Val10Glu
XM_011545781.1:c.603T>A	XP_011544083.1:p.Gly201=
XM_011545782.1:c.29T>A	XP_011544084.1:p.Val10Glu
XM_005255233.5:c.29T>A	XP_005255290.1:p.Val10Glu
XM_011545782.2:c.29T>A	XP_011544084.1:p.Val10Glu
XM_024450221.1:c.600T>A	XP_024305989.1:p.Gly200=
NM_004960.4:c.609T>A MANE Select	NP_004951.1:p.Gly203=