Canonical Allele Identifier: CA1977534959

Gene: BEST1 FTH1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61960041C= , CM000673.2:g.61960041C=	GRCh38
NC_000011.9:g.61727513C= , CM000673.1:g.61727513C=	GRCh37
NC_000011.8:g.61484089C=	NCBI36
NG_009033.1:g.15158C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.1098C= (BEST1) MANE Select	ENSP00000367282.4:p.Ile366=
ENST00000378043.8:c.1098C= (BEST1)	ENSP00000367282.4:p.Ile366=
ENST00000449131.6:c.918C= (BEST1)	ENSP00000399709.2:p.Ile306=
ENST00000524877.5:n.2729C= (BEST1)
ENST00000524926.5:c.1301C= (BEST1)	ENSP00000432681.1:p.Ser434=
ENST00000526988.1:c.983C= (BEST1)	ENSP00000433195.1:p.Ser328=
ENST00000529191.5:c.115-114G= (FTH1)	ENSP00000431659.1:n.115-114G=
ENST00000529631.5:c.115-137G= (FTH1)	ENSP00000431575.1:n.115-137G=
ENST00000530019.5:c.262-137G= (FTH1)	ENSP00000433470.1:n.262-137G=
ENST00000534553.5:c.164-2214C= (BEST1)	ENSP00000431189.1:n.164-2214C=
NM_001139443.1:c.918C= (BEST1)	NP_001132915.1:p.Ile306=
NM_001300786.1:c.837C= (BEST1)	NP_001287715.1:p.Ile279=
NM_001300787.1:c.918C= (BEST1)	NP_001287716.1:p.Ile306=
NM_004183.3:c.1098C= (BEST1)	NP_004174.1:p.Ile366=
XM_005274210.2:c.1098C= (BEST1)	XP_005274267.1:p.Ile366=
XM_005274215.2:c.780C= (BEST1)	XP_005274272.1:p.Ile260=
XM_005274216.2:c.1121C= (BEST1)	XP_005274273.1:p.Ser374=
XM_005274218.3:c.983C= (BEST1)	XP_005274275.1:p.Ser328=
XM_005274219.2:c.867+1743C= (BEST1)	XP_005274276.1:n.867+1743C=
XM_005274221.2:c.715-2214C= (BEST1)	XP_005274278.1:n.715-2214C=
XM_011545229.1:c.1098C= (BEST1)	XP_011543531.1:p.Ile366=
XM_011545230.1:c.1005C= (BEST1)	XP_011543532.1:p.Ile335=
XM_011545231.1:c.780C= (BEST1)	XP_011543533.1:p.Ile260=
XM_011545232.1:c.1301C= (BEST1)	XP_011543534.1:p.Ser434=
XM_011545233.1:c.255C= (BEST1)	XP_011543535.1:p.Ile85=
NM_001363591.1:c.780C= (BEST1)	NP_001350520.1:p.Ile260=
NM_001363592.1:c.1301C= (BEST1)	NP_001350521.1:p.Ser434=
NM_001363593.1:c.126C= (BEST1)	NP_001350522.1:p.Ile42=
NR_134580.1:n.1881C= (BEST1)
XM_005274210.4:c.1098C= (BEST1)	XP_005274267.1:p.Ile366=
XM_005274215.4:c.780C= (BEST1)	XP_005274272.1:p.Ile260=
XM_005274216.4:c.1121C= (BEST1)	XP_005274273.1:p.Ser374=
XM_005274219.4:c.867+1743C= (BEST1)	XP_005274276.1:n.867+1743C=
XM_005274221.4:c.715-2214C= (BEST1)	XP_005274278.1:n.715-2214C=
XM_011545229.3:c.1098C= (BEST1)	XP_011543531.1:p.Ile366=
XM_011545230.3:c.1005C= (BEST1)	XP_011543532.1:p.Ile335=
XM_011545233.3:c.255C= (BEST1)	XP_011543535.1:p.Ile85=
XM_017018230.2:c.983C= (BEST1)	XP_016873719.1:p.Ser328=
XR_001747952.2:n.1799C= (BEST1)
XR_001747953.2:n.1557+1743C= (BEST1)
XR_001747954.2:n.1405-2214C= (BEST1)
NM_004183.4:c.1098C= (BEST1) MANE Select	NP_004174.1:p.Ile366=
NM_001139443.2:c.918C= (BEST1)	NP_001132915.1:p.Ile306=
NM_001300786.2:c.837C= (BEST1)	NP_001287715.1:p.Ile279=
NM_001300787.2:c.918C= (BEST1)	NP_001287716.1:p.Ile306=
NM_001363591.2:c.780C= (BEST1)	NP_001350520.1:p.Ile260=
NM_001363593.2:c.126C= (BEST1)	NP_001350522.1:p.Ile42=
NR_134580.2:n.1414C= (BEST1)