Canonical Allele Identifier: CA383239132

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680663A>T (hg19) ; chr11:g.128810768A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810768A>T , CM000673.2:g.128810768A>T	GRCh38
NC_000011.9:g.128680663A>T , CM000673.1:g.128680663A>T	GRCh37
NC_000011.8:g.128185873A>T	NCBI36
NG_032912.1:g.129234A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1160A>T	ENSP00000513017.1:p.Lys387Met
ENST00000527786.7:c.1139A>T MANE Select	ENSP00000433488.2:p.Lys380Met
ENST00000281428.12:c.941A>T	ENSP00000281428.8:p.Lys314Met
ENST00000344954.10:c.560A>T	ENSP00000339627.7:p.Lys187Met
ENST00000429175.7:c.*1061A>T	ENSP00000399985.3:n.*1061A>T
ENST00000527786.6:c.1139A>T	ENSP00000433488.2:p.Lys380Met
ENST00000528790.1:n.3722A>T
ENST00000534087.3:c.1040A>T	ENSP00000432950.1:p.Lys347Met
ENST00000608303.5:c.*531A>T	ENSP00000477262.1:n.*531A>T
NM_001167681.2:c.1040A>T	NP_001161153.1:p.Lys347Met
NM_001271010.1:c.941A>T	NP_001257939.1:p.Lys314Met
NM_001271012.1:c.560A>T	NP_001257941.1:p.Lys187Met
NM_002017.4:c.1139A>T	NP_002008.2:p.Lys380Met
XM_011542701.1:c.1040A>T	XP_011541003.1:p.Lys347Met
XM_011542702.1:c.1013A>T	XP_011541004.1:p.Lys338Met
XM_011542701.2:c.1040A>T	XP_011541003.1:p.Lys347Met
XM_017017405.1:c.1040A>T	XP_016872894.1:p.Lys347Met
XM_017017406.1:c.1040A>T	XP_016872895.1:p.Lys347Met
NM_002017.5:c.1139A>T MANE Select	NP_002008.2:p.Lys380Met
NM_001167681.3:c.1040A>T	NP_001161153.1:p.Lys347Met
NM_001271010.2:c.941A>T	NP_001257939.1:p.Lys314Met
NM_001271012.2:c.560A>T	NP_001257941.1:p.Lys187Met