Canonical Allele Identifier: CA494928798

Gene: FUS

Linked Data

• gnomAD v4: 16-31185054-T-C
• MyVariant Identifiers: chr16:g.31196375T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185054T>C , CM000678.2:g.31185054T>C	GRCh38
NC_000016.9:g.31196375T>C , CM000678.1:g.31196375T>C	GRCh37
NC_000016.8:g.31103876T>C	NCBI36
NG_012889.2:g.9923T>C , LRG_655:g.9923T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.639T>C MANE Select	ENSP00000254108.8:p.Arg213=
ENST00000254108.11:c.639T>C	ENSP00000254108.7:p.Arg213=
ENST00000380244.7:c.636T>C	ENSP00000369594.3:p.Arg212=
ENST00000487509.6:n.704T>C
ENST00000566605.5:c.639T>C	ENSP00000455073.1:p.Arg213=
ENST00000568685.1:c.639T>C	ENSP00000455282.1:p.Arg213=
NM_001170634.1:c.636T>C	NP_001164105.1:p.Arg212=
NM_001170937.1:c.627T>C	NP_001164408.1:p.Arg209=
NM_004960.3:c.639T>C , LRG_655t1:c.639T>C	NP_004951.1:p.Arg213=
NR_028388.2:n.744T>C
XM_005255233.3:c.59T>C	XP_005255290.1:p.Val20Ala
XM_011545781.1:c.633T>C	XP_011544083.1:p.Arg211=
XM_011545782.1:c.59T>C	XP_011544084.1:p.Val20Ala
XM_005255233.5:c.59T>C	XP_005255290.1:p.Val20Ala
XM_011545782.2:c.59T>C	XP_011544084.1:p.Val20Ala
XM_024450221.1:c.630T>C	XP_024305989.1:p.Arg210=
NM_004960.4:c.639T>C MANE Select	NP_004951.1:p.Arg213=