Canonical Allele Identifier: CA16621534
Gene: FLI1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424633
ClinVar RCV Id: RCV000487469 RCV002526993
dbSNP Id: rs1064797084
MyVariant Identifiers: chr11:g.128680552A>G (hg19) chr11:g.128810657A>G (hg38)
PubMed: PMID:24100448
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810657A>G , CM000673.2:g.128810657A>G GRCh38
NC_000011.9:g.128680552A>G , CM000673.1:g.128680552A>G GRCh37
NC_000011.8:g.128185762A>G NCBI36
NG_032912.1:g.129123A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696982.1:c.1049A>G ENSP00000513017.1:p.Tyr350Cys
ENST00000527786.7:c.1028A>G MANE Select ENSP00000433488.2:p.Tyr343Cys
ENST00000281428.12:c.830A>G ENSP00000281428.8:p.Tyr277Cys
ENST00000344954.10:c.449A>G ENSP00000339627.7:p.Tyr150Cys
ENST00000429175.7:c.*950A>G ENSP00000399985.3:n.*950A>G
ENST00000527786.6:c.1028A>G ENSP00000433488.2:p.Tyr343Cys
ENST00000528790.1:n.3611A>G
ENST00000534087.3:c.929A>G ENSP00000432950.1:p.Tyr310Cys
ENST00000608303.5:c.*420A>G ENSP00000477262.1:n.*420A>G
NM_001167681.2:c.929A>G NP_001161153.1:p.Tyr310Cys
NM_001271010.1:c.830A>G NP_001257939.1:p.Tyr277Cys
NM_001271012.1:c.449A>G NP_001257941.1:p.Tyr150Cys
NM_002017.4:c.1028A>G NP_002008.2:p.Tyr343Cys
XM_011542701.1:c.929A>G XP_011541003.1:p.Tyr310Cys
XM_011542702.1:c.902A>G XP_011541004.1:p.Tyr301Cys
XM_011542701.2:c.929A>G XP_011541003.1:p.Tyr310Cys
XM_017017405.1:c.929A>G XP_016872894.1:p.Tyr310Cys
XM_017017406.1:c.929A>G XP_016872895.1:p.Tyr310Cys
NM_002017.5:c.1028A>G MANE Select NP_002008.2:p.Tyr343Cys
NM_001167681.3:c.929A>G NP_001161153.1:p.Tyr310Cys
NM_001271010.2:c.830A>G NP_001257939.1:p.Tyr277Cys
NM_001271012.2:c.449A>G NP_001257941.1:p.Tyr150Cys
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