Canonical Allele Identifier: CA2792344614

Gene: FTH1 BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964565_61964566del , CM000673.2:g.61964565_61964566del	GRCh38
NC_000011.9:g.61732037_61732038del , CM000673.1:g.61732037_61732038del	GRCh37
NC_000011.8:g.61488613_61488614del	NCBI36
NG_008346.1:g.8095_8096del
NG_009033.1:g.19682_19683del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273550.12:c.*161_*162del (FTH1) MANE Select	ENSP00000273550.7:n.*161_*162del
ENST00000273550.11:c.*161_*162del (FTH1)	ENSP00000273550.7:n.*161_*162del
ENST00000449131.6:c.*1416_*1417del (BEST1)	ENSP00000399709.2:n.*1416_*1417del
ENST00000529191.5:c.114+2746_114+2747del (FTH1)	ENSP00000431659.1:n.114+2746_114+2747del
ENST00000529631.5:c.114+2746_114+2747del (FTH1)	ENSP00000431575.1:n.114+2746_114+2747del
ENST00000530019.5:c.261+803_261+804del (FTH1)	ENSP00000433470.1:n.261+803_261+804del
NM_002032.2:c.*161_*162del (FTH1)	NP_002023.2:n.*161_*162del
NM_002032.3:c.*161_*162del (FTH1) MANE Select	NP_002023.2:n.*161_*162del
NM_001139443.2:c.*1416_*1417del (BEST1)	NP_001132915.1:n.*1416_*1417del
NM_001363591.2:c.*1416_*1417del (BEST1)	NP_001350520.1:n.*1416_*1417del
NM_001363593.2:c.*1416_*1417del (BEST1)	NP_001350522.1:n.*1416_*1417del