Canonical Allele Identifier: CA2008248595

Gene: FLI1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128810783_128810786delinsTCTC , CM000673.2:g.128810783_128810786delinsTCTC	GRCh38
NC_000011.9:g.128680678_128680681delinsTCTC , CM000673.1:g.128680678_128680681delinsTCTC	GRCh37
NC_000011.8:g.128185888_128185891delinsTCTC	NCBI36
NG_032912.1:g.129249_129252delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696982.1:c.1175_1178delinsTCTC	ENSP00000513017.1:p.Ile392=
ENST00000527786.7:c.1154_1157delinsTCTC MANE Select	ENSP00000433488.2:p.Ile385=
ENST00000281428.12:c.956_959delinsTCTC	ENSP00000281428.8:p.Ile319=
ENST00000344954.10:c.575_578delinsTCTC	ENSP00000339627.7:p.Ile192=
ENST00000429175.7:c.*1076_*1079delinsTCTC	ENSP00000399985.3:n.*1076_*1079delinsTCTC
ENST00000527786.6:c.1154_1157delinsTCTC	ENSP00000433488.2:p.Ile385=
ENST00000528790.1:n.3737_3740delinsTCTC
ENST00000534087.3:c.1055_1058delinsTCTC	ENSP00000432950.1:p.Ile352=
ENST00000608303.5:c.*546_*549delinsTCTC	ENSP00000477262.1:n.*546_*549delinsTCTC
NM_001167681.2:c.1055_1058delinsTCTC	NP_001161153.1:p.Ile352=
NM_001271010.1:c.956_959delinsTCTC	NP_001257939.1:p.Ile319=
NM_001271012.1:c.575_578delinsTCTC	NP_001257941.1:p.Ile192=
NM_002017.4:c.1154_1157delinsTCTC	NP_002008.2:p.Ile385=
XM_011542701.1:c.1055_1058delinsTCTC	XP_011541003.1:p.Ile352=
XM_011542702.1:c.1028_1031delinsTCTC	XP_011541004.1:p.Ile343=
XM_011542701.2:c.1055_1058delinsTCTC	XP_011541003.1:p.Ile352=
XM_017017405.1:c.1055_1058delinsTCTC	XP_016872894.1:p.Ile352=
XM_017017406.1:c.1055_1058delinsTCTC	XP_016872895.1:p.Ile352=
NM_002017.5:c.1154_1157delinsTCTC MANE Select	NP_002008.2:p.Ile385=
NM_001167681.3:c.1055_1058delinsTCTC	NP_001161153.1:p.Ile352=
NM_001271010.2:c.956_959delinsTCTC	NP_001257939.1:p.Ile319=
NM_001271012.2:c.575_578delinsTCTC	NP_001257941.1:p.Ile192=