Canonical Allele Identifier: CA2216944207

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31184859_31184869delinsGTCAAACCTTT , CM000678.2:g.31184859_31184869delinsGTCAAACCTTT	GRCh38
NC_000016.9:g.31196180_31196190delinsGTCAAACCTTT , CM000678.1:g.31196180_31196190delinsGTCAAACCTTT	GRCh37
NC_000016.8:g.31103681_31103691delinsGTCAAACCTTT	NCBI36
NG_012889.2:g.9728_9738delinsGTCAAACCTTT , LRG_655:g.9728_9738delinsGTCAAACCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.524-80_524-70delinsGTCAAACCTTT MANE Select	ENSP00000254108.8:n.524-80_524-70delinsGTCAAACCTTT
ENST00000254108.11:c.524-80_524-70delinsGTCAAACCTTT	ENSP00000254108.7:n.524-80_524-70delinsGTCAAACCTTT
ENST00000380244.7:c.521-80_521-70delinsGTCAAACCTTT	ENSP00000369594.3:n.521-80_521-70delinsGTCAAACCTTT
ENST00000487509.6:n.589-80_589-70delinsGTCAAACCTTT
ENST00000566605.5:c.524-80_524-70delinsGTCAAACCTTT	ENSP00000455073.1:n.524-80_524-70delinsGTCAAACCTTT
ENST00000568685.1:c.524-80_524-70delinsGTCAAACCTTT	ENSP00000455282.1:n.524-80_524-70delinsGTCAAACCTTT
NM_001170634.1:c.521-80_521-70delinsGTCAAACCTTT	NP_001164105.1:n.521-80_521-70delinsGTCAAACCTTT
NM_001170937.1:c.512-80_512-70delinsGTCAAACCTTT	NP_001164408.1:n.512-80_512-70delinsGTCAAACCTTT
NM_004960.3:c.524-80_524-70delinsGTCAAACCTTT , LRG_655t1:c.524-80_524-70delinsGTCAAACCTTT	NP_004951.1:n.524-80_524-70delinsGTCAAACCTTT
NR_028388.2:n.629-80_629-70delinsGTCAAACCTTT
XM_005255233.3:c.-57-80_-57-70delinsGTCAAACCTTT	XP_005255290.1:n.-57-80_-57-70delinsGTCAAACCTTT
XM_011545781.1:c.518-80_518-70delinsGTCAAACCTTT	XP_011544083.1:n.518-80_518-70delinsGTCAAACCTTT
XM_011545782.1:c.-57-80_-57-70delinsGTCAAACCTTT	XP_011544084.1:n.-57-80_-57-70delinsGTCAAACCTTT
XM_005255233.5:c.-57-80_-57-70delinsGTCAAACCTTT	XP_005255290.1:n.-57-80_-57-70delinsGTCAAACCTTT
XM_011545782.2:c.-57-80_-57-70delinsGTCAAACCTTT	XP_011544084.1:n.-57-80_-57-70delinsGTCAAACCTTT
XM_024450221.1:c.515-80_515-70delinsGTCAAACCTTT	XP_024305989.1:n.515-80_515-70delinsGTCAAACCTTT
NM_004960.4:c.524-80_524-70delinsGTCAAACCTTT MANE Select	NP_004951.1:n.524-80_524-70delinsGTCAAACCTTT