Canonical Allele Identifier: CA2632839989

Gene: FUS

Linked Data

• gnomAD v4: 16-31189349-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189349G>C , CM000678.2:g.31189349G>C	GRCh38
NC_000016.9:g.31200670G>C , CM000678.1:g.31200670G>C	GRCh37
NC_000016.8:g.31108171G>C	NCBI36
NG_012889.2:g.14218G>C , LRG_655:g.14218G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.936+123G>C MANE Select	ENSP00000254108.8:n.936+123G>C
ENST00000254108.11:c.936+123G>C	ENSP00000254108.7:n.936+123G>C
ENST00000380244.7:c.933+123G>C	ENSP00000369594.3:n.933+123G>C
ENST00000474990.5:n.230+123G>C
ENST00000487509.6:n.4111+123G>C
ENST00000564766.1:n.760+123G>C
ENST00000566605.5:c.*109+123G>C	ENSP00000455073.1:n.*109+123G>C
ENST00000568685.1:c.939+123G>C	ENSP00000455282.1:n.939+123G>C
ENST00000568901.2:n.310+123G>C
NM_001170634.1:c.933+123G>C	NP_001164105.1:n.933+123G>C
NM_001170937.1:c.924+123G>C	NP_001164408.1:n.924+123G>C
NM_004960.3:c.936+123G>C , LRG_655t1:c.936+123G>C	NP_004951.1:n.936+123G>C
NR_028388.2:n.1006+123G>C
XM_005255233.3:c.321+123G>C	XP_005255290.1:n.321+123G>C
XM_011545781.1:c.930+123G>C	XP_011544083.1:n.930+123G>C
XM_011545782.1:c.321+123G>C	XP_011544084.1:n.321+123G>C
XM_005255233.5:c.321+123G>C	XP_005255290.1:n.321+123G>C
XM_011545782.2:c.321+123G>C	XP_011544084.1:n.321+123G>C
XM_024450221.1:c.927+123G>C	XP_024305989.1:n.927+123G>C
NM_004960.4:c.936+123G>C MANE Select	NP_004951.1:n.936+123G>C