Canonical Allele Identifier: CA395672265

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200498T>G (hg19) ; chr16:g.31189177T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189177T>G , CM000678.2:g.31189177T>G	GRCh38
NC_000016.9:g.31200498T>G , CM000678.1:g.31200498T>G	GRCh37
NC_000016.8:g.31107999T>G	NCBI36
NG_012889.2:g.14046T>G , LRG_655:g.14046T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.887T>G MANE Select	ENSP00000254108.8:p.Val296Gly
ENST00000254108.11:c.887T>G	ENSP00000254108.7:p.Val296Gly
ENST00000380244.7:c.884T>G	ENSP00000369594.3:p.Val295Gly
ENST00000474990.5:n.181T>G
ENST00000487509.6:n.4062T>G
ENST00000564766.1:n.711T>G
ENST00000566605.5:c.*60T>G	ENSP00000455073.1:n.*60T>G
ENST00000568685.1:c.890T>G	ENSP00000455282.1:p.Val297Gly
ENST00000568901.2:n.261T>G
NM_001170634.1:c.884T>G	NP_001164105.1:p.Val295Gly
NM_001170937.1:c.875T>G	NP_001164408.1:p.Val292Gly
NM_004960.3:c.887T>G , LRG_655t1:c.887T>G	NP_004951.1:p.Val296Gly
NR_028388.2:n.957T>G
XM_005255233.3:c.272T>G	XP_005255290.1:p.Val91Gly
XM_011545781.1:c.881T>G	XP_011544083.1:p.Val294Gly
XM_011545782.1:c.272T>G	XP_011544084.1:p.Val91Gly
XM_005255233.5:c.272T>G	XP_005255290.1:p.Val91Gly
XM_011545782.2:c.272T>G	XP_011544084.1:p.Val91Gly
XM_024450221.1:c.878T>G	XP_024305989.1:p.Val293Gly
NM_004960.4:c.887T>G MANE Select	NP_004951.1:p.Val296Gly