Canonical Allele Identifier: CA383238844

Gene: FLI1

Linked Data

• MyVariant Identifiers: chr11:g.128680539C>G (hg19) ; chr11:g.128810644C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810644C>G , CM000673.2:g.128810644C>G	GRCh38
NC_000011.9:g.128680539C>G , CM000673.1:g.128680539C>G	GRCh37
NC_000011.8:g.128185749C>G	NCBI36
NG_032912.1:g.129110C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696982.1:c.1036C>G	ENSP00000513017.1:p.Leu346Val
ENST00000527786.7:c.1015C>G MANE Select	ENSP00000433488.2:p.Leu339Val
ENST00000281428.12:c.817C>G	ENSP00000281428.8:p.Leu273Val
ENST00000344954.10:c.436C>G	ENSP00000339627.7:p.Leu146Val
ENST00000429175.7:c.*937C>G	ENSP00000399985.3:n.*937C>G
ENST00000527786.6:c.1015C>G	ENSP00000433488.2:p.Leu339Val
ENST00000528790.1:n.3598C>G
ENST00000534087.3:c.916C>G	ENSP00000432950.1:p.Leu306Val
ENST00000608303.5:c.*407C>G	ENSP00000477262.1:n.*407C>G
NM_001167681.2:c.916C>G	NP_001161153.1:p.Leu306Val
NM_001271010.1:c.817C>G	NP_001257939.1:p.Leu273Val
NM_001271012.1:c.436C>G	NP_001257941.1:p.Leu146Val
NM_002017.4:c.1015C>G	NP_002008.2:p.Leu339Val
XM_011542701.1:c.916C>G	XP_011541003.1:p.Leu306Val
XM_011542702.1:c.889C>G	XP_011541004.1:p.Leu297Val
XM_011542701.2:c.916C>G	XP_011541003.1:p.Leu306Val
XM_017017405.1:c.916C>G	XP_016872894.1:p.Leu306Val
XM_017017406.1:c.916C>G	XP_016872895.1:p.Leu306Val
NM_002017.5:c.1015C>G MANE Select	NP_002008.2:p.Leu339Val
NM_001167681.3:c.916C>G	NP_001161153.1:p.Leu306Val
NM_001271010.2:c.817C>G	NP_001257939.1:p.Leu273Val
NM_001271012.2:c.436C>G	NP_001257941.1:p.Leu146Val