Canonical Allele Identifier: CA8023688

Gene: FUS

Linked Data

• dbSNP Id: rs754668657
• ExAC: 16:31196229 T / C
• gnomAD v2: 16-31196229-T-C
• gnomAD v4: 16-31184908-T-C
• MyVariant Identifiers: chr16:g.31196229T>C (hg19) ; chr16:g.31184908T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184908T>C , CM000678.2:g.31184908T>C	GRCh38
NC_000016.9:g.31196229T>C , CM000678.1:g.31196229T>C	GRCh37
NC_000016.8:g.31103730T>C	NCBI36
NG_012889.2:g.9777T>C , LRG_655:g.9777T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-31T>C MANE Select	ENSP00000254108.8:n.524-31T>C
ENST00000254108.11:c.524-31T>C	ENSP00000254108.7:n.524-31T>C
ENST00000380244.7:c.521-31T>C	ENSP00000369594.3:n.521-31T>C
ENST00000487509.6:n.589-31T>C
ENST00000566605.5:c.524-31T>C	ENSP00000455073.1:n.524-31T>C
ENST00000568685.1:c.524-31T>C	ENSP00000455282.1:n.524-31T>C
NM_001170634.1:c.521-31T>C	NP_001164105.1:n.521-31T>C
NM_001170937.1:c.512-31T>C	NP_001164408.1:n.512-31T>C
NM_004960.3:c.524-31T>C , LRG_655t1:c.524-31T>C	NP_004951.1:n.524-31T>C
NR_028388.2:n.629-31T>C
XM_005255233.3:c.-57-31T>C	XP_005255290.1:n.-57-31T>C
XM_011545781.1:c.518-31T>C	XP_011544083.1:n.518-31T>C
XM_011545782.1:c.-57-31T>C	XP_011544084.1:n.-57-31T>C
XM_005255233.5:c.-57-31T>C	XP_005255290.1:n.-57-31T>C
XM_011545782.2:c.-57-31T>C	XP_011544084.1:n.-57-31T>C
XM_024450221.1:c.515-31T>C	XP_024305989.1:n.515-31T>C
NM_004960.4:c.524-31T>C MANE Select	NP_004951.1:n.524-31T>C