Canonical Allele Identifier: CA380853676

Gene: FTH1 BEST1

Linked Data

• MyVariant Identifiers: chr11:g.61732242A>C (hg19) ; chr11:g.61964770A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964770A>C , CM000673.2:g.61964770A>C	GRCh38
NC_000011.9:g.61732242A>C , CM000673.1:g.61732242A>C	GRCh37
NC_000011.8:g.61488818A>C	NCBI36
NG_008346.1:g.7891T>G
NG_009033.1:g.19887A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620041.5:c.509T>G (FTH1)	ENSP00000484477.1:p.Leu170Arg
ENST00000273550.12:c.509T>G (FTH1) MANE Select	ENSP00000273550.7:p.Leu170Arg
ENST00000273550.11:c.509T>G (FTH1)	ENSP00000273550.7:p.Leu170Arg
ENST00000449131.6:c.*1621A>C (BEST1)	ENSP00000399709.2:n.*1621A>C
ENST00000526640.5:c.419T>G (FTH1)	ENSP00000433321.1:p.Leu140Arg
ENST00000529191.5:c.114+2542T>G (FTH1)	ENSP00000431659.1:n.114+2542T>G
ENST00000529631.5:c.114+2542T>G (FTH1)	ENSP00000431575.1:n.114+2542T>G
ENST00000530019.5:c.261+599T>G (FTH1)	ENSP00000433470.1:n.261+599T>G
ENST00000532601.1:c.299T>G (FTH1)	ENSP00000435111.1:p.Leu100Arg
ENST00000532829.5:c.*214T>G (FTH1)	ENSP00000432223.1:n.*214T>G
ENST00000534180.1:c.*418T>G (FTH1)	ENSP00000434403.1:n.*418T>G
ENST00000534719.1:n.765T>G (FTH1)
ENST00000620041.4:c.509T>G (FTH1)	ENSP00000484477.1:p.Leu170Arg
NM_002032.2:c.509T>G (FTH1)	NP_002023.2:p.Leu170Arg
NM_002032.3:c.509T>G (FTH1) MANE Select	NP_002023.2:p.Leu170Arg
NM_001139443.2:c.*1621A>C (BEST1)	NP_001132915.1:n.*1621A>C
NM_001363591.2:c.*1621A>C (BEST1)	NP_001350520.1:n.*1621A>C
NM_001363593.2:c.*1621A>C (BEST1)	NP_001350522.1:n.*1621A>C