Canonical Allele Identifier: CA13433224

Gene: FLI1 SENCR

Linked Data

• dbSNP Id: rs7930515
• gnomAD v2: 11-128564794-A-C
• gnomAD v3: 11-128694899-A-C
• gnomAD v4: 11-128694899-A-C
• MyVariant Identifiers: chr11:g.128564794A>C (hg19) ; chr11:g.128694899A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128694899A>C , CM000673.2:g.128694899A>C	GRCh38
NC_000011.9:g.128564794A>C , CM000673.1:g.128564794A>C	GRCh37
NC_000011.8:g.128070004A>C	NCBI36
NG_032912.1:g.13365A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.39+8198A>C (FLI1)	ENSP00000513017.1:n.39+8198A>C
ENST00000527786.7:c.18+623A>C (FLI1) MANE Select	ENSP00000433488.2:n.18+623A>C
ENST00000281428.12:c.-352+623A>C (FLI1)	ENSP00000281428.8:n.-352+623A>C
ENST00000344954.10:c.-203+8198A>C (FLI1)	ENSP00000339627.7:n.-203+8198A>C
ENST00000429175.7:c.18+623A>C (FLI1)	ENSP00000399985.3:n.18+623A>C
ENST00000527767.7:c.-82+1756A>C (FLI1)	ENSP00000476428.1:n.-82+1756A>C
ENST00000527786.6:c.18+623A>C (FLI1)	ENSP00000433488.2:n.18+623A>C
ENST00000534087.3:c.-136+623A>C (FLI1)	ENSP00000432950.1:n.-136+623A>C
ENST00000608303.5:c.-82+8198A>C (FLI1)	ENSP00000477262.1:n.-82+8198A>C
NM_001167681.2:c.-136+623A>C (FLI1)	NP_001161153.1:n.-136+623A>C
NM_001271010.1:c.-352+623A>C (FLI1)	NP_001257939.1:n.-352+623A>C
NM_001271012.1:c.-203+8198A>C (FLI1)	NP_001257941.1:n.-203+8198A>C
NM_002017.4:c.18+623A>C (FLI1)	NP_002008.2:n.18+623A>C
NR_038908.1:n.111+1014T>G (SENCR)
XM_011542701.1:c.-82+1756A>C (FLI1)	XP_011541003.1:n.-82+1756A>C
XM_011542702.1:c.18+623A>C (FLI1)	XP_011541004.1:n.18+623A>C
XM_011542701.2:c.-82+1756A>C (FLI1)	XP_011541003.1:n.-82+1756A>C
XM_017017405.1:c.-82+9527A>C (FLI1)	XP_016872894.1:n.-82+9527A>C
XM_017017406.1:c.-82+2099A>C (FLI1)	XP_016872895.1:n.-82+2099A>C
NM_002017.5:c.18+623A>C (FLI1) MANE Select	NP_002008.2:n.18+623A>C
NM_001167681.3:c.-136+623A>C (FLI1)	NP_001161153.1:n.-136+623A>C
NM_001271010.2:c.-352+623A>C (FLI1)	NP_001257939.1:n.-352+623A>C
NM_001271012.2:c.-203+8198A>C (FLI1)	NP_001257941.1:n.-203+8198A>C