Canonical Allele Identifier: CA2632839877

Gene: FUS

Linked Data

• gnomAD v4: 16-31189072-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189072T>A , CM000678.2:g.31189072T>A	GRCh38
NC_000016.9:g.31200393T>A , CM000678.1:g.31200393T>A	GRCh37
NC_000016.8:g.31107894T>A	NCBI36
NG_012889.2:g.13941T>A , LRG_655:g.13941T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.833-51T>A MANE Select	ENSP00000254108.8:n.833-51T>A
ENST00000254108.11:c.833-51T>A	ENSP00000254108.7:n.833-51T>A
ENST00000380244.7:c.830-51T>A	ENSP00000369594.3:n.830-51T>A
ENST00000474990.5:n.127-51T>A
ENST00000487509.6:n.4008-51T>A
ENST00000564766.1:n.606T>A
ENST00000566605.5:c.*6-51T>A	ENSP00000455073.1:n.*6-51T>A
ENST00000568685.1:c.833-48T>A	ENSP00000455282.1:n.833-48T>A
ENST00000568901.2:n.207-51T>A
NM_001170634.1:c.830-51T>A	NP_001164105.1:n.830-51T>A
NM_001170937.1:c.821-51T>A	NP_001164408.1:n.821-51T>A
NM_004960.3:c.833-51T>A , LRG_655t1:c.833-51T>A	NP_004951.1:n.833-51T>A
NR_028388.2:n.903-51T>A
XM_005255233.3:c.218-51T>A	XP_005255290.1:n.218-51T>A
XM_011545781.1:c.827-51T>A	XP_011544083.1:n.827-51T>A
XM_011545782.1:c.218-51T>A	XP_011544084.1:n.218-51T>A
XM_005255233.5:c.218-51T>A	XP_005255290.1:n.218-51T>A
XM_011545782.2:c.218-51T>A	XP_011544084.1:n.218-51T>A
XM_024450221.1:c.824-51T>A	XP_024305989.1:n.824-51T>A
NM_004960.4:c.833-51T>A MANE Select	NP_004951.1:n.833-51T>A