Canonical Allele Identifier: CA383238855
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810650T>A , CM000673.2:g.128810650T>A GRCh38
NC_000011.9:g.128680545T>A , CM000673.1:g.128680545T>A GRCh37
NC_000011.8:g.128185755T>A NCBI36
NG_032912.1:g.129116T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696982.1:c.1042T>A ENSP00000513017.1:p.Tyr348Asn
ENST00000527786.7:c.1021T>A MANE Select ENSP00000433488.2:p.Tyr341Asn
ENST00000281428.12:c.823T>A ENSP00000281428.8:p.Tyr275Asn
ENST00000344954.10:c.442T>A ENSP00000339627.7:p.Tyr148Asn
ENST00000429175.7:c.*943T>A ENSP00000399985.3:n.*943T>A
ENST00000527786.6:c.1021T>A ENSP00000433488.2:p.Tyr341Asn
ENST00000528790.1:n.3604T>A
ENST00000534087.3:c.922T>A ENSP00000432950.1:p.Tyr308Asn
ENST00000608303.5:c.*413T>A ENSP00000477262.1:n.*413T>A
NM_001167681.2:c.922T>A NP_001161153.1:p.Tyr308Asn
NM_001271010.1:c.823T>A NP_001257939.1:p.Tyr275Asn
NM_001271012.1:c.442T>A NP_001257941.1:p.Tyr148Asn
NM_002017.4:c.1021T>A NP_002008.2:p.Tyr341Asn
XM_011542701.1:c.922T>A XP_011541003.1:p.Tyr308Asn
XM_011542702.1:c.895T>A XP_011541004.1:p.Tyr299Asn
XM_011542701.2:c.922T>A XP_011541003.1:p.Tyr308Asn
XM_017017405.1:c.922T>A XP_016872894.1:p.Tyr308Asn
XM_017017406.1:c.922T>A XP_016872895.1:p.Tyr308Asn
NM_002017.5:c.1021T>A MANE Select NP_002008.2:p.Tyr341Asn
NM_001167681.3:c.922T>A NP_001161153.1:p.Tyr308Asn
NM_001271010.2:c.823T>A NP_001257939.1:p.Tyr275Asn
NM_001271012.2:c.442T>A NP_001257941.1:p.Tyr148Asn