Canonical Allele Identifier: CA395672472

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200534T>C (hg19) ; chr16:g.31189213T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189213T>C , CM000678.2:g.31189213T>C	GRCh38
NC_000016.9:g.31200534T>C , CM000678.1:g.31200534T>C	GRCh37
NC_000016.8:g.31108035T>C	NCBI36
NG_012889.2:g.14082T>C , LRG_655:g.14082T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.923T>C MANE Select	ENSP00000254108.8:p.Ile308Thr
ENST00000254108.11:c.923T>C	ENSP00000254108.7:p.Ile308Thr
ENST00000380244.7:c.920T>C	ENSP00000369594.3:p.Ile307Thr
ENST00000474990.5:n.217T>C
ENST00000487509.6:n.4098T>C
ENST00000564766.1:n.747T>C
ENST00000566605.5:c.*96T>C	ENSP00000455073.1:n.*96T>C
ENST00000568685.1:c.926T>C	ENSP00000455282.1:p.Ile309Thr
ENST00000568901.2:n.297T>C
NM_001170634.1:c.920T>C	NP_001164105.1:p.Ile307Thr
NM_001170937.1:c.911T>C	NP_001164408.1:p.Ile304Thr
NM_004960.3:c.923T>C , LRG_655t1:c.923T>C	NP_004951.1:p.Ile308Thr
NR_028388.2:n.993T>C
XM_005255233.3:c.308T>C	XP_005255290.1:p.Ile103Thr
XM_011545781.1:c.917T>C	XP_011544083.1:p.Ile306Thr
XM_011545782.1:c.308T>C	XP_011544084.1:p.Ile103Thr
XM_005255233.5:c.308T>C	XP_005255290.1:p.Ile103Thr
XM_011545782.2:c.308T>C	XP_011544084.1:p.Ile103Thr
XM_024450221.1:c.914T>C	XP_024305989.1:p.Ile305Thr
NM_004960.4:c.923T>C MANE Select	NP_004951.1:p.Ile308Thr