Canonical Allele Identifier: CA2792344577

Gene: FTH1 BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964475_61964478del , CM000673.2:g.61964475_61964478del	GRCh38
NC_000011.9:g.61731947_61731950del , CM000673.1:g.61731947_61731950del	GRCh37
NC_000011.8:g.61488523_61488526del	NCBI36
NG_008346.1:g.8184_8187del
NG_009033.1:g.19592_19595del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273550.12:c.*250_*253del (FTH1) MANE Select	ENSP00000273550.7:n.*250_*253del
ENST00000273550.11:c.*250_*253del (FTH1)	ENSP00000273550.7:n.*250_*253del
ENST00000449131.6:c.*1326_*1329del (BEST1)	ENSP00000399709.2:n.*1326_*1329del
ENST00000529191.5:c.114+2835_114+2838del (FTH1)	ENSP00000431659.1:n.114+2835_114+2838del
ENST00000529631.5:c.114+2835_114+2838del (FTH1)	ENSP00000431575.1:n.114+2835_114+2838del
ENST00000530019.5:c.261+892_261+895del (FTH1)	ENSP00000433470.1:n.261+892_261+895del
NM_002032.2:c.*250_*253del (FTH1)	NP_002023.2:n.*250_*253del
NM_002032.3:c.*250_*253del (FTH1) MANE Select	NP_002023.2:n.*250_*253del
NM_001139443.2:c.*1326_*1329del (BEST1)	NP_001132915.1:n.*1326_*1329del
NM_001363591.2:c.*1326_*1329del (BEST1)	NP_001350520.1:n.*1326_*1329del
NM_001363593.2:c.*1326_*1329del (BEST1)	NP_001350522.1:n.*1326_*1329del