Canonical Allele Identifier: CA383239113
Gene: FLI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810761A>C , CM000673.2:g.128810761A>C GRCh38
NC_000011.9:g.128680656A>C , CM000673.1:g.128680656A>C GRCh37
NC_000011.8:g.128185866A>C NCBI36
NG_032912.1:g.129227A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.1153A>C ENSP00000513017.1:p.Met385Leu
ENST00000527786.7:c.1132A>C MANE Select ENSP00000433488.2:p.Met378Leu
ENST00000281428.12:c.934A>C ENSP00000281428.8:p.Met312Leu
ENST00000344954.10:c.553A>C ENSP00000339627.7:p.Met185Leu
ENST00000429175.7:c.*1054A>C ENSP00000399985.3:n.*1054A>C
ENST00000527786.6:c.1132A>C ENSP00000433488.2:p.Met378Leu
ENST00000528790.1:n.3715A>C
ENST00000534087.3:c.1033A>C ENSP00000432950.1:p.Met345Leu
ENST00000608303.5:c.*524A>C ENSP00000477262.1:n.*524A>C
NM_001167681.2:c.1033A>C NP_001161153.1:p.Met345Leu
NM_001271010.1:c.934A>C NP_001257939.1:p.Met312Leu
NM_001271012.1:c.553A>C NP_001257941.1:p.Met185Leu
NM_002017.4:c.1132A>C NP_002008.2:p.Met378Leu
XM_011542701.1:c.1033A>C XP_011541003.1:p.Met345Leu
XM_011542702.1:c.1006A>C XP_011541004.1:p.Met336Leu
XM_011542701.2:c.1033A>C XP_011541003.1:p.Met345Leu
XM_017017405.1:c.1033A>C XP_016872894.1:p.Met345Leu
XM_017017406.1:c.1033A>C XP_016872895.1:p.Met345Leu
NM_002017.5:c.1132A>C MANE Select NP_002008.2:p.Met378Leu
NM_001167681.3:c.1033A>C NP_001161153.1:p.Met345Leu
NM_001271010.2:c.934A>C NP_001257939.1:p.Met312Leu
NM_001271012.2:c.553A>C NP_001257941.1:p.Met185Leu