Canonical Allele Identifier: CA395672362

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200515G>T (hg19) ; chr16:g.31189194G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189194G>T , CM000678.2:g.31189194G>T	GRCh38
NC_000016.9:g.31200515G>T , CM000678.1:g.31200515G>T	GRCh37
NC_000016.8:g.31108016G>T	NCBI36
NG_012889.2:g.14063G>T , LRG_655:g.14063G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.904G>T MANE Select	ENSP00000254108.8:p.Ala302Ser
ENST00000254108.11:c.904G>T	ENSP00000254108.7:p.Ala302Ser
ENST00000380244.7:c.901G>T	ENSP00000369594.3:p.Ala301Ser
ENST00000474990.5:n.198G>T
ENST00000487509.6:n.4079G>T
ENST00000564766.1:n.728G>T
ENST00000566605.5:c.*77G>T	ENSP00000455073.1:n.*77G>T
ENST00000568685.1:c.907G>T	ENSP00000455282.1:p.Ala303Ser
ENST00000568901.2:n.278G>T
NM_001170634.1:c.901G>T	NP_001164105.1:p.Ala301Ser
NM_001170937.1:c.892G>T	NP_001164408.1:p.Ala298Ser
NM_004960.3:c.904G>T , LRG_655t1:c.904G>T	NP_004951.1:p.Ala302Ser
NR_028388.2:n.974G>T
XM_005255233.3:c.289G>T	XP_005255290.1:p.Ala97Ser
XM_011545781.1:c.898G>T	XP_011544083.1:p.Ala300Ser
XM_011545782.1:c.289G>T	XP_011544084.1:p.Ala97Ser
XM_005255233.5:c.289G>T	XP_005255290.1:p.Ala97Ser
XM_011545782.2:c.289G>T	XP_011544084.1:p.Ala97Ser
XM_024450221.1:c.895G>T	XP_024305989.1:p.Ala299Ser
NM_004960.4:c.904G>T MANE Select	NP_004951.1:p.Ala302Ser