Canonical Allele Identifier: CA383238693

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680473G>A (hg19) ; chr11:g.128810578G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810578G>A , CM000673.2:g.128810578G>A	GRCh38
NC_000011.9:g.128680473G>A , CM000673.1:g.128680473G>A	GRCh37
NC_000011.8:g.128185683G>A	NCBI36
NG_032912.1:g.129044G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.970G>A	ENSP00000513017.1:p.Val324Met
ENST00000527786.7:c.949G>A MANE Select	ENSP00000433488.2:p.Val317Met
ENST00000281428.12:c.751G>A	ENSP00000281428.8:p.Val251Met
ENST00000344954.10:c.370G>A	ENSP00000339627.7:p.Val124Met
ENST00000429175.7:c.*871G>A	ENSP00000399985.3:n.*871G>A
ENST00000527786.6:c.949G>A	ENSP00000433488.2:p.Val317Met
ENST00000528790.1:n.3532G>A
ENST00000534087.3:c.850G>A	ENSP00000432950.1:p.Val284Met
ENST00000608303.5:c.*341G>A	ENSP00000477262.1:n.*341G>A
NM_001167681.2:c.850G>A	NP_001161153.1:p.Val284Met
NM_001271010.1:c.751G>A	NP_001257939.1:p.Val251Met
NM_001271012.1:c.370G>A	NP_001257941.1:p.Val124Met
NM_002017.4:c.949G>A	NP_002008.2:p.Val317Met
XM_011542701.1:c.850G>A	XP_011541003.1:p.Val284Met
XM_011542702.1:c.823G>A	XP_011541004.1:p.Val275Met
XM_011542701.2:c.850G>A	XP_011541003.1:p.Val284Met
XM_017017405.1:c.850G>A	XP_016872894.1:p.Val284Met
XM_017017406.1:c.850G>A	XP_016872895.1:p.Val284Met
NM_002017.5:c.949G>A MANE Select	NP_002008.2:p.Val317Met
NM_001167681.3:c.850G>A	NP_001161153.1:p.Val284Met
NM_001271010.2:c.751G>A	NP_001257939.1:p.Val251Met
NM_001271012.2:c.370G>A	NP_001257941.1:p.Val124Met