Canonical Allele Identifier: CA395672211

Gene: FUS

Linked Data

• MyVariant Identifiers: chr16:g.31200492A>C (hg19) ; chr16:g.31189171A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31189171A>C , CM000678.2:g.31189171A>C	GRCh38
NC_000016.9:g.31200492A>C , CM000678.1:g.31200492A>C	GRCh37
NC_000016.8:g.31107993A>C	NCBI36
NG_012889.2:g.14040A>C , LRG_655:g.14040A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254108.12:c.881A>C MANE Select	ENSP00000254108.8:p.Glu294Ala
ENST00000254108.11:c.881A>C	ENSP00000254108.7:p.Glu294Ala
ENST00000380244.7:c.878A>C	ENSP00000369594.3:p.Glu293Ala
ENST00000474990.5:n.175A>C
ENST00000487509.6:n.4056A>C
ENST00000564766.1:n.705A>C
ENST00000566605.5:c.*54A>C	ENSP00000455073.1:n.*54A>C
ENST00000568685.1:c.884A>C	ENSP00000455282.1:p.Glu295Ala
ENST00000568901.2:n.255A>C
NM_001170634.1:c.878A>C	NP_001164105.1:p.Glu293Ala
NM_001170937.1:c.869A>C	NP_001164408.1:p.Glu290Ala
NM_004960.3:c.881A>C , LRG_655t1:c.881A>C	NP_004951.1:p.Glu294Ala
NR_028388.2:n.951A>C
XM_005255233.3:c.266A>C	XP_005255290.1:p.Glu89Ala
XM_011545781.1:c.875A>C	XP_011544083.1:p.Glu292Ala
XM_011545782.1:c.266A>C	XP_011544084.1:p.Glu89Ala
XM_005255233.5:c.266A>C	XP_005255290.1:p.Glu89Ala
XM_011545782.2:c.266A>C	XP_011544084.1:p.Glu89Ala
XM_024450221.1:c.872A>C	XP_024305989.1:p.Glu291Ala
NM_004960.4:c.881A>C MANE Select	NP_004951.1:p.Glu294Ala