Canonical Allele Identifier: CA1977534688

Gene: BEST1 FTH1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959923A= , CM000673.2:g.61959923A=	GRCh38
NC_000011.9:g.61727395A= , CM000673.1:g.61727395A=	GRCh37
NC_000011.8:g.61483971A=	NCBI36
NG_009033.1:g.15040A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.980A= (BEST1) MANE Select	ENSP00000367282.4:p.Gln327=
ENST00000378043.8:c.980A= (BEST1)	ENSP00000367282.4:p.Gln327=
ENST00000449131.6:c.800A= (BEST1)	ENSP00000399709.2:p.Gln267=
ENST00000524877.5:n.2611A= (BEST1)
ENST00000524926.5:c.1183A= (BEST1)	ENSP00000432681.1:p.Arg395=
ENST00000526988.1:c.865A= (BEST1)	ENSP00000433195.1:p.Arg289=
ENST00000529191.5:c.119T= (FTH1)	ENSP00000431659.1:p.Leu40=
ENST00000529631.5:c.115-19T= (FTH1)	ENSP00000431575.1:n.115-19T=
ENST00000530019.5:c.262-19T= (FTH1)	ENSP00000433470.1:n.262-19T=
ENST00000534553.5:c.164-2332A= (BEST1)	ENSP00000431189.1:n.164-2332A=
NM_001139443.1:c.800A= (BEST1)	NP_001132915.1:p.Gln267=
NM_001300786.1:c.719A= (BEST1)	NP_001287715.1:p.Gln240=
NM_001300787.1:c.800A= (BEST1)	NP_001287716.1:p.Gln267=
NM_004183.3:c.980A= (BEST1)	NP_004174.1:p.Gln327=
XM_005274210.2:c.980A= (BEST1)	XP_005274267.1:p.Gln327=
XM_005274215.2:c.662A= (BEST1)	XP_005274272.1:p.Gln221=
XM_005274216.2:c.1003A= (BEST1)	XP_005274273.1:p.Arg335=
XM_005274218.3:c.865A= (BEST1)	XP_005274275.1:p.Arg289=
XM_005274219.2:c.867+1625A= (BEST1)	XP_005274276.1:n.867+1625A=
XM_005274221.2:c.715-2332A= (BEST1)	XP_005274278.1:n.715-2332A=
XM_011545229.1:c.980A= (BEST1)	XP_011543531.1:p.Gln327=
XM_011545230.1:c.887A= (BEST1)	XP_011543532.1:p.Gln296=
XM_011545231.1:c.662A= (BEST1)	XP_011543533.1:p.Gln221=
XM_011545232.1:c.1183A= (BEST1)	XP_011543534.1:p.Arg395=
XM_011545233.1:c.137A= (BEST1)	XP_011543535.1:p.Gln46=
NM_001363591.1:c.662A= (BEST1)	NP_001350520.1:p.Gln221=
NM_001363592.1:c.1183A= (BEST1)	NP_001350521.1:p.Arg395=
NM_001363593.1:c.8A= (BEST1)	NP_001350522.1:p.Gln3=
NR_134580.1:n.1763A= (BEST1)
XM_005274210.4:c.980A= (BEST1)	XP_005274267.1:p.Gln327=
XM_005274215.4:c.662A= (BEST1)	XP_005274272.1:p.Gln221=
XM_005274216.4:c.1003A= (BEST1)	XP_005274273.1:p.Arg335=
XM_005274219.4:c.867+1625A= (BEST1)	XP_005274276.1:n.867+1625A=
XM_005274221.4:c.715-2332A= (BEST1)	XP_005274278.1:n.715-2332A=
XM_011545229.3:c.980A= (BEST1)	XP_011543531.1:p.Gln327=
XM_011545230.3:c.887A= (BEST1)	XP_011543532.1:p.Gln296=
XM_011545233.3:c.137A= (BEST1)	XP_011543535.1:p.Gln46=
XM_017018230.2:c.865A= (BEST1)	XP_016873719.1:p.Arg289=
XR_001747952.2:n.1681A= (BEST1)
XR_001747953.2:n.1557+1625A= (BEST1)
XR_001747954.2:n.1405-2332A= (BEST1)
XR_001748245.1:n.5T=
XR_002957249.1:n.5T=
NM_004183.4:c.980A= (BEST1) MANE Select	NP_004174.1:p.Gln327=
NM_001139443.2:c.800A= (BEST1)	NP_001132915.1:p.Gln267=
NM_001300786.2:c.719A= (BEST1)	NP_001287715.1:p.Gln240=
NM_001300787.2:c.800A= (BEST1)	NP_001287716.1:p.Gln267=
NM_001363591.2:c.662A= (BEST1)	NP_001350520.1:p.Gln221=
NM_001363593.2:c.8A= (BEST1)	NP_001350522.1:p.Gln3=
NR_134580.2:n.1296A= (BEST1)