Canonical Allele Identifier: CA383238875

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680552A>T (hg19) ; chr11:g.128810657A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1049A>T	ENSP00000513017.1:p.Tyr350Phe
ENST00000527786.7:c.1028A>T MANE Select	ENSP00000433488.2:p.Tyr343Phe
ENST00000281428.12:c.830A>T	ENSP00000281428.8:p.Tyr277Phe
ENST00000344954.10:c.449A>T	ENSP00000339627.7:p.Tyr150Phe
ENST00000429175.7:c.*950A>T	ENSP00000399985.3:n.*950A>T
ENST00000527786.6:c.1028A>T	ENSP00000433488.2:p.Tyr343Phe
ENST00000528790.1:n.3611A>T
ENST00000534087.3:c.929A>T	ENSP00000432950.1:p.Tyr310Phe
ENST00000608303.5:c.*420A>T	ENSP00000477262.1:n.*420A>T
NM_001167681.2:c.929A>T	NP_001161153.1:p.Tyr310Phe
NM_001271010.1:c.830A>T	NP_001257939.1:p.Tyr277Phe
NM_001271012.1:c.449A>T	NP_001257941.1:p.Tyr150Phe
NM_002017.4:c.1028A>T	NP_002008.2:p.Tyr343Phe
XM_011542701.1:c.929A>T	XP_011541003.1:p.Tyr310Phe
XM_011542702.1:c.902A>T	XP_011541004.1:p.Tyr301Phe
XM_011542701.2:c.929A>T	XP_011541003.1:p.Tyr310Phe
XM_017017405.1:c.929A>T	XP_016872894.1:p.Tyr310Phe
XM_017017406.1:c.929A>T	XP_016872895.1:p.Tyr310Phe
NM_002017.5:c.1028A>T MANE Select	NP_002008.2:p.Tyr343Phe
NM_001167681.3:c.929A>T	NP_001161153.1:p.Tyr310Phe
NM_001271010.2:c.830A>T	NP_001257939.1:p.Tyr277Phe
NM_001271012.2:c.449A>T	NP_001257941.1:p.Tyr150Phe