Canonical Allele Identifier: CA395672463

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200532G>C (hg19) ; chr16:g.31189211G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189211G>C , CM000678.2:g.31189211G>C	GRCh38
NC_000016.9:g.31200532G>C , CM000678.1:g.31200532G>C	GRCh37
NC_000016.8:g.31108033G>C	NCBI36
NG_012889.2:g.14080G>C , LRG_655:g.14080G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.921G>C MANE Select	ENSP00000254108.8:p.Gln307His
ENST00000254108.11:c.921G>C	ENSP00000254108.7:p.Gln307His
ENST00000380244.7:c.918G>C	ENSP00000369594.3:p.Gln306His
ENST00000474990.5:n.215G>C
ENST00000487509.6:n.4096G>C
ENST00000564766.1:n.745G>C
ENST00000566605.5:c.*94G>C	ENSP00000455073.1:n.*94G>C
ENST00000568685.1:c.924G>C	ENSP00000455282.1:p.Gln308His
ENST00000568901.2:n.295G>C
NM_001170634.1:c.918G>C	NP_001164105.1:p.Gln306His
NM_001170937.1:c.909G>C	NP_001164408.1:p.Gln303His
NM_004960.3:c.921G>C , LRG_655t1:c.921G>C	NP_004951.1:p.Gln307His
NR_028388.2:n.991G>C
XM_005255233.3:c.306G>C	XP_005255290.1:p.Gln102His
XM_011545781.1:c.915G>C	XP_011544083.1:p.Gln305His
XM_011545782.1:c.306G>C	XP_011544084.1:p.Gln102His
XM_005255233.5:c.306G>C	XP_005255290.1:p.Gln102His
XM_011545782.2:c.306G>C	XP_011544084.1:p.Gln102His
XM_024450221.1:c.912G>C	XP_024305989.1:p.Gln304His
NM_004960.4:c.921G>C MANE Select	NP_004951.1:p.Gln307His