Canonical Allele Identifier: CA477702606
Gene: FLI1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.128680526G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128810631G>A , CM000673.2:g.128810631G>A GRCh38
NC_000011.9:g.128680526G>A , CM000673.1:g.128680526G>A GRCh37
NC_000011.8:g.128185736G>A NCBI36
NG_032912.1:g.129097G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696982.1:c.1023G>A ENSP00000513017.1:p.Lys341=
ENST00000527786.7:c.1002G>A MANE Select ENSP00000433488.2:p.Lys334=
ENST00000281428.12:c.804G>A ENSP00000281428.8:p.Lys268=
ENST00000344954.10:c.423G>A ENSP00000339627.7:p.Lys141=
ENST00000429175.7:c.*924G>A ENSP00000399985.3:n.*924G>A
ENST00000527786.6:c.1002G>A ENSP00000433488.2:p.Lys334=
ENST00000528790.1:n.3585G>A
ENST00000534087.3:c.903G>A ENSP00000432950.1:p.Lys301=
ENST00000608303.5:c.*394G>A ENSP00000477262.1:n.*394G>A
NM_001167681.2:c.903G>A NP_001161153.1:p.Lys301=
NM_001271010.1:c.804G>A NP_001257939.1:p.Lys268=
NM_001271012.1:c.423G>A NP_001257941.1:p.Lys141=
NM_002017.4:c.1002G>A NP_002008.2:p.Lys334=
XM_011542701.1:c.903G>A XP_011541003.1:p.Lys301=
XM_011542702.1:c.876G>A XP_011541004.1:p.Lys292=
XM_011542701.2:c.903G>A XP_011541003.1:p.Lys301=
XM_017017405.1:c.903G>A XP_016872894.1:p.Lys301=
XM_017017406.1:c.903G>A XP_016872895.1:p.Lys301=
NM_002017.5:c.1002G>A MANE Select NP_002008.2:p.Lys334=
NM_001167681.3:c.903G>A NP_001161153.1:p.Lys301=
NM_001271010.2:c.804G>A NP_001257939.1:p.Lys268=
NM_001271012.2:c.423G>A NP_001257941.1:p.Lys141=