Canonical Allele Identifier: CA2613931346

Gene: FTH1 BEST1

Linked Data

• gnomAD v4: 11-61964919-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964922del , CM000673.2:g.61964922del	GRCh38
NC_000011.9:g.61732394del , CM000673.1:g.61732394del	GRCh37
NC_000011.8:g.61488970del	NCBI36
NG_008346.1:g.7741del
NG_009033.1:g.20039del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620041.5:c.388-29del (FTH1)	ENSP00000484477.1:n.388-29del
ENST00000273550.12:c.388-29del (FTH1) MANE Select	ENSP00000273550.7:n.388-29del
ENST00000273550.11:c.388-29del (FTH1)	ENSP00000273550.7:n.388-29del
ENST00000449131.6:c.*1773del (BEST1)	ENSP00000399709.2:n.*1773del
ENST00000526640.5:c.298-29del (FTH1)	ENSP00000433321.1:n.298-29del
ENST00000529191.5:c.114+2392del (FTH1)	ENSP00000431659.1:n.114+2392del
ENST00000529631.5:c.114+2392del (FTH1)	ENSP00000431575.1:n.114+2392del
ENST00000530019.5:c.261+449del (FTH1)	ENSP00000433470.1:n.261+449del
ENST00000532601.1:c.178-29del (FTH1)	ENSP00000435111.1:n.178-29del
ENST00000532829.5:c.*93-29del (FTH1)	ENSP00000432223.1:n.*93-29del
ENST00000533138.1:n.832-29del (FTH1)
ENST00000534180.1:c.*297-29del (FTH1)	ENSP00000434403.1:n.*297-29del
ENST00000534719.1:n.615del (FTH1)
ENST00000620041.4:c.388-29del (FTH1)	ENSP00000484477.1:n.388-29del
NM_002032.2:c.388-29del (FTH1)	NP_002023.2:n.388-29del
NM_002032.3:c.388-29del (FTH1) MANE Select	NP_002023.2:n.388-29del
NM_001139443.2:c.*1773del (BEST1)	NP_001132915.1:n.*1773del
NM_001363591.2:c.*1773del (BEST1)	NP_001350520.1:n.*1773del
NM_001363593.2:c.*1773del (BEST1)	NP_001350522.1:n.*1773del