Canonical Allele Identifier: CA383239104

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680650T>C (hg19) ; chr11:g.128810755T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810755T>C , CM000673.2:g.128810755T>C	GRCh38
NC_000011.9:g.128680650T>C , CM000673.1:g.128680650T>C	GRCh37
NC_000011.8:g.128185860T>C	NCBI36
NG_032912.1:g.129221T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1147T>C	ENSP00000513017.1:p.Ser383Pro
ENST00000527786.7:c.1126T>C MANE Select	ENSP00000433488.2:p.Ser376Pro
ENST00000281428.12:c.928T>C	ENSP00000281428.8:p.Ser310Pro
ENST00000344954.10:c.547T>C	ENSP00000339627.7:p.Ser183Pro
ENST00000429175.7:c.*1048T>C	ENSP00000399985.3:n.*1048T>C
ENST00000527786.6:c.1126T>C	ENSP00000433488.2:p.Ser376Pro
ENST00000528790.1:n.3709T>C
ENST00000534087.3:c.1027T>C	ENSP00000432950.1:p.Ser343Pro
ENST00000608303.5:c.*518T>C	ENSP00000477262.1:n.*518T>C
NM_001167681.2:c.1027T>C	NP_001161153.1:p.Ser343Pro
NM_001271010.1:c.928T>C	NP_001257939.1:p.Ser310Pro
NM_001271012.1:c.547T>C	NP_001257941.1:p.Ser183Pro
NM_002017.4:c.1126T>C	NP_002008.2:p.Ser376Pro
XM_011542701.1:c.1027T>C	XP_011541003.1:p.Ser343Pro
XM_011542702.1:c.1000T>C	XP_011541004.1:p.Ser334Pro
XM_011542701.2:c.1027T>C	XP_011541003.1:p.Ser343Pro
XM_017017405.1:c.1027T>C	XP_016872894.1:p.Ser343Pro
XM_017017406.1:c.1027T>C	XP_016872895.1:p.Ser343Pro
NM_002017.5:c.1126T>C MANE Select	NP_002008.2:p.Ser376Pro
NM_001167681.3:c.1027T>C	NP_001161153.1:p.Ser343Pro
NM_001271010.2:c.928T>C	NP_001257939.1:p.Ser310Pro
NM_001271012.2:c.547T>C	NP_001257941.1:p.Ser183Pro