Canonical Allele Identifier: CA2792344603

Gene: FTH1 BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964538_61964539insA , CM000673.2:g.61964538_61964539insA	GRCh38
NC_000011.9:g.61732010_61732011insA , CM000673.1:g.61732010_61732011insA	GRCh37
NC_000011.8:g.61488586_61488587insA	NCBI36
NG_008346.1:g.8122_8123insT
NG_009033.1:g.19655_19656insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273550.12:c.*188_*189insT (FTH1) MANE Select	ENSP00000273550.7:n.*188_*189insT
ENST00000273550.11:c.*188_*189insT (FTH1)	ENSP00000273550.7:n.*188_*189insT
ENST00000449131.6:c.*1389_*1390insA (BEST1)	ENSP00000399709.2:n.*1389_*1390insA
ENST00000529191.5:c.114+2773_114+2774insT (FTH1)	ENSP00000431659.1:n.114+2773_114+2774insT
ENST00000529631.5:c.114+2773_114+2774insT (FTH1)	ENSP00000431575.1:n.114+2773_114+2774insT
ENST00000530019.5:c.261+830_261+831insT (FTH1)	ENSP00000433470.1:n.261+830_261+831insT
NM_002032.2:c.*188_*189insT (FTH1)	NP_002023.2:n.*188_*189insT
NM_002032.3:c.*188_*189insT (FTH1) MANE Select	NP_002023.2:n.*188_*189insT
NM_001139443.2:c.*1389_*1390insA (BEST1)	NP_001132915.1:n.*1389_*1390insA
NM_001363591.2:c.*1389_*1390insA (BEST1)	NP_001350520.1:n.*1389_*1390insA
NM_001363593.2:c.*1389_*1390insA (BEST1)	NP_001350522.1:n.*1389_*1390insA