Canonical Allele Identifier: CA2632839998

Gene: FUS

Linked Data

• gnomAD v4: 16-31189358-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189358G>A , CM000678.2:g.31189358G>A	GRCh38
NC_000016.9:g.31200679G>A , CM000678.1:g.31200679G>A	GRCh37
NC_000016.8:g.31108180G>A	NCBI36
NG_012889.2:g.14227G>A , LRG_655:g.14227G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+132G>A MANE Select	ENSP00000254108.8:n.936+132G>A
ENST00000254108.11:c.936+132G>A	ENSP00000254108.7:n.936+132G>A
ENST00000380244.7:c.933+132G>A	ENSP00000369594.3:n.933+132G>A
ENST00000474990.5:n.230+132G>A
ENST00000487509.6:n.4111+132G>A
ENST00000564766.1:n.760+132G>A
ENST00000566605.5:c.*109+132G>A	ENSP00000455073.1:n.*109+132G>A
ENST00000568685.1:c.939+132G>A	ENSP00000455282.1:n.939+132G>A
ENST00000568901.2:n.310+132G>A
NM_001170634.1:c.933+132G>A	NP_001164105.1:n.933+132G>A
NM_001170937.1:c.924+132G>A	NP_001164408.1:n.924+132G>A
NM_004960.3:c.936+132G>A , LRG_655t1:c.936+132G>A	NP_004951.1:n.936+132G>A
NR_028388.2:n.1006+132G>A
XM_005255233.3:c.321+132G>A	XP_005255290.1:n.321+132G>A
XM_011545781.1:c.930+132G>A	XP_011544083.1:n.930+132G>A
XM_011545782.1:c.321+132G>A	XP_011544084.1:n.321+132G>A
XM_005255233.5:c.321+132G>A	XP_005255290.1:n.321+132G>A
XM_011545782.2:c.321+132G>A	XP_011544084.1:n.321+132G>A
XM_024450221.1:c.927+132G>A	XP_024305989.1:n.927+132G>A
NM_004960.4:c.936+132G>A MANE Select	NP_004951.1:n.936+132G>A