Canonical Allele Identifier: CA494715326

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31202715T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191394T>G , CM000678.2:g.31191394T>G	GRCh38
NC_000016.9:g.31202715T>G , CM000678.1:g.31202715T>G	GRCh37
NC_000016.8:g.31110216T>G	NCBI36
NG_012889.2:g.16263T>G , LRG_655:g.16263T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.1542-5T>G MANE Select	ENSP00000254108.8:n.1542-5T>G
ENST00000254108.11:c.1542-5T>G	ENSP00000254108.7:n.1542-5T>G
ENST00000380244.7:c.1539-5T>G	ENSP00000369594.3:n.1539-5T>G
ENST00000483853.1:n.619-5T>G
ENST00000487509.6:n.4717-5T>G
ENST00000566605.5:c.*715-5T>G	ENSP00000455073.1:n.*715-5T>G
ENST00000568685.1:c.1545-5T>G	ENSP00000455282.1:n.1545-5T>G
ENST00000569760.5:n.433-5T>G
NM_001170634.1:c.1539-5T>G	NP_001164105.1:n.1539-5T>G
NM_001170937.1:c.1530-5T>G	NP_001164408.1:n.1530-5T>G
NM_004960.3:c.1542-5T>G , LRG_655t1:c.1542-5T>G	NP_004951.1:n.1542-5T>G
NR_028388.2:n.1612-5T>G
XM_005255233.3:c.927-5T>G	XP_005255290.1:n.927-5T>G
XM_011545781.1:c.1536-5T>G	XP_011544083.1:n.1536-5T>G
XM_011545782.1:c.927-5T>G	XP_011544084.1:n.927-5T>G
XM_005255233.5:c.927-5T>G	XP_005255290.1:n.927-5T>G
XM_011545782.2:c.927-5T>G	XP_011544084.1:n.927-5T>G
XM_024450221.1:c.1533-5T>G	XP_024305989.1:n.1533-5T>G
NM_004960.4:c.1542-5T>G MANE Select	NP_004951.1:n.1542-5T>G