Canonical Allele Identifier: CA477702614

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680538C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810643C>T , CM000673.2:g.128810643C>T	GRCh38
NC_000011.9:g.128680538C>T , CM000673.1:g.128680538C>T	GRCh37
NC_000011.8:g.128185748C>T	NCBI36
NG_032912.1:g.129109C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.1035C>T	ENSP00000513017.1:p.Ala345=
ENST00000527786.7:c.1014C>T MANE Select	ENSP00000433488.2:p.Ala338=
ENST00000281428.12:c.816C>T	ENSP00000281428.8:p.Ala272=
ENST00000344954.10:c.435C>T	ENSP00000339627.7:p.Ala145=
ENST00000429175.7:c.*936C>T	ENSP00000399985.3:n.*936C>T
ENST00000527786.6:c.1014C>T	ENSP00000433488.2:p.Ala338=
ENST00000528790.1:n.3597C>T
ENST00000534087.3:c.915C>T	ENSP00000432950.1:p.Ala305=
ENST00000608303.5:c.*406C>T	ENSP00000477262.1:n.*406C>T
NM_001167681.2:c.915C>T	NP_001161153.1:p.Ala305=
NM_001271010.1:c.816C>T	NP_001257939.1:p.Ala272=
NM_001271012.1:c.435C>T	NP_001257941.1:p.Ala145=
NM_002017.4:c.1014C>T	NP_002008.2:p.Ala338=
XM_011542701.1:c.915C>T	XP_011541003.1:p.Ala305=
XM_011542702.1:c.888C>T	XP_011541004.1:p.Ala296=
XM_011542701.2:c.915C>T	XP_011541003.1:p.Ala305=
XM_017017405.1:c.915C>T	XP_016872894.1:p.Ala305=
XM_017017406.1:c.915C>T	XP_016872895.1:p.Ala305=
NM_002017.5:c.1014C>T MANE Select	NP_002008.2:p.Ala338=
NM_001167681.3:c.915C>T	NP_001161153.1:p.Ala305=
NM_001271010.2:c.816C>T	NP_001257939.1:p.Ala272=
NM_001271012.2:c.435C>T	NP_001257941.1:p.Ala145=