Canonical Allele Identifier: CA13474237
Gene: FLI1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128712662T>C , CM000673.2:g.128712662T>C GRCh38
NC_000011.9:g.128582557T>C , CM000673.1:g.128582557T>C GRCh37
NC_000011.8:g.128087767T>C NCBI36
NG_032912.1:g.31128T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.39+25961T>C ENSP00000513017.1:n.39+25961T>C
ENST00000527786.7:c.18+18386T>C MANE Select ENSP00000433488.2:n.18+18386T>C
ENST00000281428.12:c.-352+18386T>C ENSP00000281428.8:n.-352+18386T>C
ENST00000344954.10:c.-203+25961T>C ENSP00000339627.7:n.-203+25961T>C
ENST00000429175.7:c.18+18386T>C ENSP00000399985.3:n.18+18386T>C
ENST00000527767.7:c.-82+19519T>C ENSP00000476428.1:n.-82+19519T>C
ENST00000527786.6:c.18+18386T>C ENSP00000433488.2:n.18+18386T>C
ENST00000534087.3:c.-136+18386T>C ENSP00000432950.1:n.-136+18386T>C
ENST00000608303.5:c.-82+25961T>C ENSP00000477262.1:n.-82+25961T>C
NM_001167681.2:c.-136+18386T>C NP_001161153.1:n.-136+18386T>C
NM_001271010.1:c.-352+18386T>C NP_001257939.1:n.-352+18386T>C
NM_001271012.1:c.-203+25961T>C NP_001257941.1:n.-203+25961T>C
NM_002017.4:c.18+18386T>C NP_002008.2:n.18+18386T>C
XM_011542701.1:c.-82+19519T>C XP_011541003.1:n.-82+19519T>C
XM_011542702.1:c.18+18386T>C XP_011541004.1:n.18+18386T>C
XM_011542701.2:c.-82+19519T>C XP_011541003.1:n.-82+19519T>C
XM_017017405.1:c.-82+27290T>C XP_016872894.1:n.-82+27290T>C
XM_017017406.1:c.-82+19862T>C XP_016872895.1:n.-82+19862T>C
NM_002017.5:c.18+18386T>C MANE Select NP_002008.2:n.18+18386T>C
NM_001167681.3:c.-136+18386T>C NP_001161153.1:n.-136+18386T>C
NM_001271010.2:c.-352+18386T>C NP_001257939.1:n.-352+18386T>C
NM_001271012.2:c.-203+25961T>C NP_001257941.1:n.-203+25961T>C
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