Canonical Allele Identifier: CA494715333

Gene: FUS

Linked Data

• gnomAD v4: 16-31191402-T-C
• MyVariant Identifiers: chr16:g.31202723T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31191402T>C , CM000678.2:g.31191402T>C	GRCh38
NC_000016.9:g.31202723T>C , CM000678.1:g.31202723T>C	GRCh37
NC_000016.8:g.31110224T>C	NCBI36
NG_012889.2:g.16271T>C , LRG_655:g.16271T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.1545T>C MANE Select	ENSP00000254108.8:p.Gly515=
ENST00000254108.11:c.1545T>C	ENSP00000254108.7:p.Gly515=
ENST00000380244.7:c.1542T>C	ENSP00000369594.3:p.Gly514=
ENST00000483853.1:n.622T>C
ENST00000487509.6:n.4720T>C
ENST00000566605.5:c.*718T>C	ENSP00000455073.1:n.*718T>C
ENST00000568685.1:c.1548T>C	ENSP00000455282.1:p.Gly516=
ENST00000569760.5:n.436T>C
NM_001170634.1:c.1542T>C	NP_001164105.1:p.Gly514=
NM_001170937.1:c.1533T>C	NP_001164408.1:p.Gly511=
NM_004960.3:c.1545T>C , LRG_655t1:c.1545T>C	NP_004951.1:p.Gly515=
NR_028388.2:n.1615T>C
XM_005255233.3:c.930T>C	XP_005255290.1:p.Gly310=
XM_011545781.1:c.1539T>C	XP_011544083.1:p.Gly513=
XM_011545782.1:c.930T>C	XP_011544084.1:p.Gly310=
XM_005255233.5:c.930T>C	XP_005255290.1:p.Gly310=
XM_011545782.2:c.930T>C	XP_011544084.1:p.Gly310=
XM_024450221.1:c.1536T>C	XP_024305989.1:p.Gly512=
NM_004960.4:c.1545T>C MANE Select	NP_004951.1:p.Gly515=