Canonical Allele Identifier: CA2008248451

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810667_128810670delinsCATT , CM000673.2:g.128810667_128810670delinsCATT	GRCh38
NC_000011.9:g.128680562_128680565delinsCATT , CM000673.1:g.128680562_128680565delinsCATT	GRCh37
NC_000011.8:g.128185772_128185775delinsCATT	NCBI36
NG_032912.1:g.129133_129136delinsCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1059_1062delinsCATT	ENSP00000513017.1:p.Asn353=
ENST00000527786.7:c.1038_1041delinsCATT MANE Select	ENSP00000433488.2:p.Asn346=
ENST00000281428.12:c.840_843delinsCATT	ENSP00000281428.8:p.Asn280=
ENST00000344954.10:c.459_462delinsCATT	ENSP00000339627.7:p.Asn153=
ENST00000429175.7:c.*960_*963delinsCATT	ENSP00000399985.3:n.*960_*963delinsCATT
ENST00000527786.6:c.1038_1041delinsCATT	ENSP00000433488.2:p.Asn346=
ENST00000528790.1:n.3621_3624delinsCATT
ENST00000534087.3:c.939_942delinsCATT	ENSP00000432950.1:p.Asn313=
ENST00000608303.5:c.*430_*433delinsCATT	ENSP00000477262.1:n.*430_*433delinsCATT
NM_001167681.2:c.939_942delinsCATT	NP_001161153.1:p.Asn313=
NM_001271010.1:c.840_843delinsCATT	NP_001257939.1:p.Asn280=
NM_001271012.1:c.459_462delinsCATT	NP_001257941.1:p.Asn153=
NM_002017.4:c.1038_1041delinsCATT	NP_002008.2:p.Asn346=
XM_011542701.1:c.939_942delinsCATT	XP_011541003.1:p.Asn313=
XM_011542702.1:c.912_915delinsCATT	XP_011541004.1:p.Asn304=
XM_011542701.2:c.939_942delinsCATT	XP_011541003.1:p.Asn313=
XM_017017405.1:c.939_942delinsCATT	XP_016872894.1:p.Asn313=
XM_017017406.1:c.939_942delinsCATT	XP_016872895.1:p.Asn313=
NM_002017.5:c.1038_1041delinsCATT MANE Select	NP_002008.2:p.Asn346=
NM_001167681.3:c.939_942delinsCATT	NP_001161153.1:p.Asn313=
NM_001271010.2:c.840_843delinsCATT	NP_001257939.1:p.Asn280=
NM_001271012.2:c.459_462delinsCATT	NP_001257941.1:p.Asn153=