Canonical Allele Identifier: CA2613931139

Gene: FTH1 BEST1

Linked Data

• gnomAD v4: 11-61964422-CTGCCCAAACTAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61964425_61964436del , CM000673.2:g.61964425_61964436del	GRCh38
NC_000011.9:g.61731897_61731908del , CM000673.1:g.61731897_61731908del	GRCh37
NC_000011.8:g.61488473_61488484del	NCBI36
NG_008346.1:g.8227_8238del
NG_009033.1:g.19542_19553del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273550.12:c.*293_*304del (FTH1) MANE Select	ENSP00000273550.7:n.*293_*304del
ENST00000378043.9:c.*303_*314del (BEST1) MANE Select	ENSP00000367282.4:n.*303_*314del
ENST00000273550.11:c.*293_*304del (FTH1)	ENSP00000273550.7:n.*293_*304del
ENST00000378043.8:c.*303_*314del (BEST1)	ENSP00000367282.4:n.*303_*314del
ENST00000449131.6:c.*1276_*1287del (BEST1)	ENSP00000399709.2:n.*1276_*1287del
ENST00000524926.5:c.*956_*967del (BEST1)	ENSP00000432681.1:n.*956_*967del
ENST00000529191.5:c.114+2878_114+2889del (FTH1)	ENSP00000431659.1:n.114+2878_114+2889del
ENST00000529631.5:c.114+2878_114+2889del (FTH1)	ENSP00000431575.1:n.114+2878_114+2889del
ENST00000530019.5:c.261+935_261+946del (FTH1)	ENSP00000433470.1:n.261+935_261+946del
NM_001300786.1:c.*303_*314del (BEST1)	NP_001287715.1:n.*303_*314del
NM_001300787.1:c.*303_*314del (BEST1)	NP_001287716.1:n.*303_*314del
NM_002032.2:c.*293_*304del (FTH1)	NP_002023.2:n.*293_*304del
NM_004183.3:c.*303_*314del (BEST1)	NP_004174.1:n.*303_*314del
XM_005274210.2:c.*1276_*1287del (BEST1)	XP_005274267.1:n.*1276_*1287del
XM_005274215.2:c.*303_*314del (BEST1)	XP_005274272.1:n.*303_*314del
XM_011545229.1:c.*1276_*1287del (BEST1)	XP_011543531.1:n.*1276_*1287del
XM_011545230.1:c.*1276_*1287del (BEST1)	XP_011543532.1:n.*1276_*1287del
XM_011545231.1:c.*1276_*1287del (BEST1)	XP_011543533.1:n.*1276_*1287del
XM_011545233.1:c.*1276_*1287del (BEST1)	XP_011543535.1:n.*1276_*1287del
NM_001363591.1:c.*1276_*1287del (BEST1)	NP_001350520.1:n.*1276_*1287del
NM_001363592.1:c.*2166_*2177del (BEST1)	NP_001350521.1:n.*2166_*2177del
NM_001363593.1:c.*1276_*1287del (BEST1)	NP_001350522.1:n.*1276_*1287del
NR_134580.1:n.2844_2855del (BEST1)
XM_005274210.4:c.*1276_*1287del (BEST1)	XP_005274267.1:n.*1276_*1287del
XM_005274215.4:c.*303_*314del (BEST1)	XP_005274272.1:n.*303_*314del
XM_005274216.4:c.*2166_*2177del (BEST1)	XP_005274273.1:n.*2166_*2177del
XM_005274219.4:c.*2072_*2083del (BEST1)	XP_005274276.1:n.*2072_*2083del
XM_005274221.4:c.*2072_*2083del (BEST1)	XP_005274278.1:n.*2072_*2083del
XM_011545229.3:c.*1276_*1287del (BEST1)	XP_011543531.1:n.*1276_*1287del
XM_011545230.3:c.*1276_*1287del (BEST1)	XP_011543532.1:n.*1276_*1287del
XM_011545233.3:c.*1276_*1287del (BEST1)	XP_011543535.1:n.*1276_*1287del
XM_017018230.2:c.*2166_*2177del (BEST1)	XP_016873719.1:n.*2166_*2177del
NM_002032.3:c.*293_*304del (FTH1) MANE Select	NP_002023.2:n.*293_*304del
NM_004183.4:c.*303_*314del (BEST1) MANE Select	NP_004174.1:n.*303_*314del
NM_001139443.2:c.*1276_*1287del (BEST1)	NP_001132915.1:n.*1276_*1287del
NM_001300786.2:c.*303_*314del (BEST1)	NP_001287715.1:n.*303_*314del
NM_001300787.2:c.*303_*314del (BEST1)	NP_001287716.1:n.*303_*314del
NM_001363591.2:c.*1276_*1287del (BEST1)	NP_001350520.1:n.*1276_*1287del
NM_001363593.2:c.*1276_*1287del (BEST1)	NP_001350522.1:n.*1276_*1287del
NR_134580.2:n.2377_2388del (BEST1)