Canonical Allele Identifier: CA2792344581

Gene: FTH1 BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964495_61964497del , CM000673.2:g.61964495_61964497del	GRCh38
NC_000011.9:g.61731967_61731969del , CM000673.1:g.61731967_61731969del	GRCh37
NC_000011.8:g.61488543_61488545del	NCBI36
NG_008346.1:g.8165_8167del
NG_009033.1:g.19612_19614del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273550.12:c.*231_*233del (FTH1) MANE Select	ENSP00000273550.7:n.*231_*233del
ENST00000273550.11:c.*231_*233del (FTH1)	ENSP00000273550.7:n.*231_*233del
ENST00000449131.6:c.*1346_*1348del (BEST1)	ENSP00000399709.2:n.*1346_*1348del
ENST00000529191.5:c.114+2816_114+2818del (FTH1)	ENSP00000431659.1:n.114+2816_114+2818del
ENST00000529631.5:c.114+2816_114+2818del (FTH1)	ENSP00000431575.1:n.114+2816_114+2818del
ENST00000530019.5:c.261+873_261+875del (FTH1)	ENSP00000433470.1:n.261+873_261+875del
NM_002032.2:c.*231_*233del (FTH1)	NP_002023.2:n.*231_*233del
NM_002032.3:c.*231_*233del (FTH1) MANE Select	NP_002023.2:n.*231_*233del
NM_001139443.2:c.*1346_*1348del (BEST1)	NP_001132915.1:n.*1346_*1348del
NM_001363591.2:c.*1346_*1348del (BEST1)	NP_001350520.1:n.*1346_*1348del
NM_001363593.2:c.*1346_*1348del (BEST1)	NP_001350522.1:n.*1346_*1348del