Canonical Allele Identifier: CA395669828

Gene: FUS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31185023G>C , CM000678.2:g.31185023G>C	GRCh38
NC_000016.9:g.31196344G>C , CM000678.1:g.31196344G>C	GRCh37
NC_000016.8:g.31103845G>C	NCBI36
NG_012889.2:g.9892G>C , LRG_655:g.9892G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004960.4:c.608G>C MANE Select	NP_004951.1:p.Gly203Ala
ENST00000254108.12:c.608G>C MANE Select	ENSP00000254108.8:p.Gly203Ala
NM_001170634.1:c.605G>C	NP_001164105.1:p.Gly202Ala
NM_001170937.1:c.596G>C	NP_001164408.1:p.Gly199Ala
NM_004960.3:c.608G>C , LRG_655t1:c.608G>C	NP_004951.1:p.Gly203Ala
NR_028388.2:n.713G>C
ENST00000254108.11:c.608G>C	ENSP00000254108.7:p.Gly203Ala
ENST00000380244.7:c.605G>C	ENSP00000369594.3:p.Gly202Ala
ENST00000487509.6:n.673G>C
ENST00000566605.5:c.608G>C	ENSP00000455073.1:p.Gly203Ala
ENST00000568685.1:c.608G>C	ENSP00000455282.1:p.Gly203Ala
XM_005255233.3:c.28G>C	XP_005255290.1:p.Val10Leu
XM_005255233.5:c.28G>C	XP_005255290.1:p.Val10Leu
XM_011545781.1:c.602G>C	XP_011544083.1:p.Gly201Ala
XM_011545782.1:c.28G>C	XP_011544084.1:p.Val10Leu
XM_011545782.2:c.28G>C	XP_011544084.1:p.Val10Leu
XM_024450221.1:c.599G>C	XP_024305989.1:p.Gly200Ala