Canonical Allele Identifier: CA8023683

Gene: FUS

Linked Data

• dbSNP Id: rs113171066
• ExAC: 16:31196224 G / GTT
• gnomAD v2: 16-31196224-G-GTT
• gnomAD v3: 16-31184903-G-GTT
• gnomAD v4: 16-31184903-G-GTT
• MyVariant Identifiers: chr16:g.31196226_31196227insTT (hg19) ; chr16:g.31196224_31196225insTT (hg19) ; chr16:g.31184903_31184904insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184914_31184915dup , CM000678.2:g.31184914_31184915dup	GRCh38
NC_000016.9:g.31196235_31196236dup , CM000678.1:g.31196235_31196236dup	GRCh37
NC_000016.8:g.31103736_31103737dup	NCBI36
NG_012889.2:g.9783_9784dup , LRG_655:g.9783_9784dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-25_524-24dup MANE Select	ENSP00000254108.8:n.524-25_524-24dup
ENST00000254108.11:c.524-25_524-24dup	ENSP00000254108.7:n.524-25_524-24dup
ENST00000380244.7:c.521-25_521-24dup	ENSP00000369594.3:n.521-25_521-24dup
ENST00000487509.6:n.589-25_589-24dup
ENST00000566605.5:c.524-25_524-24dup	ENSP00000455073.1:n.524-25_524-24dup
ENST00000568685.1:c.524-25_524-24dup	ENSP00000455282.1:n.524-25_524-24dup
NM_001170634.1:c.521-25_521-24dup	NP_001164105.1:n.521-25_521-24dup
NM_001170937.1:c.512-25_512-24dup	NP_001164408.1:n.512-25_512-24dup
NM_004960.3:c.524-25_524-24dup , LRG_655t1:c.524-25_524-24dup	NP_004951.1:n.524-25_524-24dup
NR_028388.2:n.629-25_629-24dup
XM_005255233.3:c.-57-25_-57-24dup	XP_005255290.1:n.-57-25_-57-24dup
XM_011545781.1:c.518-25_518-24dup	XP_011544083.1:n.518-25_518-24dup
XM_011545782.1:c.-57-25_-57-24dup	XP_011544084.1:n.-57-25_-57-24dup
XM_005255233.5:c.-57-25_-57-24dup	XP_005255290.1:n.-57-25_-57-24dup
XM_011545782.2:c.-57-25_-57-24dup	XP_011544084.1:n.-57-25_-57-24dup
XM_024450221.1:c.515-25_515-24dup	XP_024305989.1:n.515-25_515-24dup
NM_004960.4:c.524-25_524-24dup MANE Select	NP_004951.1:n.524-25_524-24dup