Canonical Allele Identifier: CA222946121

Gene: FTH1 BEST1

Linked Data

• dbSNP Id: rs773410863
• gnomAD v2: 11-61732167-AC-A
• gnomAD v4: 11-61964695-AC-A
• MyVariant Identifiers: chr11:g.61732168del (hg19) ; chr11:g.61964696del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964699del , CM000673.2:g.61964699del	GRCh38
NC_000011.9:g.61732171del , CM000673.1:g.61732171del	GRCh37
NC_000011.8:g.61488747del	NCBI36
NG_008346.1:g.7965del
NG_009033.1:g.19816del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620041.5:c.*31del (FTH1)	ENSP00000484477.1:n.*31del
ENST00000273550.12:c.*31del (FTH1) MANE Select	ENSP00000273550.7:n.*31del
ENST00000273550.11:c.*31del (FTH1)	ENSP00000273550.7:n.*31del
ENST00000449131.6:c.*1550del (BEST1)	ENSP00000399709.2:n.*1550del
ENST00000526640.5:c.*31del (FTH1)	ENSP00000433321.1:n.*31del
ENST00000529191.5:c.114+2616del (FTH1)	ENSP00000431659.1:n.114+2616del
ENST00000529631.5:c.114+2616del (FTH1)	ENSP00000431575.1:n.114+2616del
ENST00000530019.5:c.261+673del (FTH1)	ENSP00000433470.1:n.261+673del
ENST00000532601.1:c.*31del (FTH1)	ENSP00000435111.1:n.*31del
ENST00000532829.5:c.*288del (FTH1)	ENSP00000432223.1:n.*288del
ENST00000534180.1:c.*492del (FTH1)	ENSP00000434403.1:n.*492del
ENST00000620041.4:c.*31del (FTH1)	ENSP00000484477.1:n.*31del
NM_002032.2:c.*31del (FTH1)	NP_002023.2:n.*31del
NM_002032.3:c.*31del (FTH1) MANE Select	NP_002023.2:n.*31del
NM_001139443.2:c.*1550del (BEST1)	NP_001132915.1:n.*1550del
NM_001363591.2:c.*1550del (BEST1)	NP_001350520.1:n.*1550del
NM_001363593.2:c.*1550del (BEST1)	NP_001350522.1:n.*1550del