Canonical Allele Identifier: CA1977534773

Gene: BEST1 FTH1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959961A= , CM000673.2:g.61959961A=	GRCh38
NC_000011.9:g.61727433A= , CM000673.1:g.61727433A=	GRCh37
NC_000011.8:g.61484009A=	NCBI36
NG_009033.1:g.15078A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.1018A= (BEST1) MANE Select	ENSP00000367282.4:p.Lys340=
ENST00000378043.8:c.1018A= (BEST1)	ENSP00000367282.4:p.Lys340=
ENST00000449131.6:c.838A= (BEST1)	ENSP00000399709.2:p.Lys280=
ENST00000524877.5:n.2649A= (BEST1)
ENST00000524926.5:c.1221A= (BEST1)	ENSP00000432681.1:p.Ile407=
ENST00000526988.1:c.903A= (BEST1)	ENSP00000433195.1:p.Ile301=
ENST00000529191.5:c.115-34T= (FTH1)	ENSP00000431659.1:n.115-34T=
ENST00000529631.5:c.115-57T= (FTH1)	ENSP00000431575.1:n.115-57T=
ENST00000530019.5:c.262-57T= (FTH1)	ENSP00000433470.1:n.262-57T=
ENST00000534553.5:c.164-2294A= (BEST1)	ENSP00000431189.1:n.164-2294A=
NM_001139443.1:c.838A= (BEST1)	NP_001132915.1:p.Lys280=
NM_001300786.1:c.757A= (BEST1)	NP_001287715.1:p.Lys253=
NM_001300787.1:c.838A= (BEST1)	NP_001287716.1:p.Lys280=
NM_004183.3:c.1018A= (BEST1)	NP_004174.1:p.Lys340=
XM_005274210.2:c.1018A= (BEST1)	XP_005274267.1:p.Lys340=
XM_005274215.2:c.700A= (BEST1)	XP_005274272.1:p.Lys234=
XM_005274216.2:c.1041A= (BEST1)	XP_005274273.1:p.Ile347=
XM_005274218.3:c.903A= (BEST1)	XP_005274275.1:p.Ile301=
XM_005274219.2:c.867+1663A= (BEST1)	XP_005274276.1:n.867+1663A=
XM_005274221.2:c.715-2294A= (BEST1)	XP_005274278.1:n.715-2294A=
XM_011545229.1:c.1018A= (BEST1)	XP_011543531.1:p.Lys340=
XM_011545230.1:c.925A= (BEST1)	XP_011543532.1:p.Lys309=
XM_011545231.1:c.700A= (BEST1)	XP_011543533.1:p.Lys234=
XM_011545232.1:c.1221A= (BEST1)	XP_011543534.1:p.Ile407=
XM_011545233.1:c.175A= (BEST1)	XP_011543535.1:p.Lys59=
NM_001363591.1:c.700A= (BEST1)	NP_001350520.1:p.Lys234=
NM_001363592.1:c.1221A= (BEST1)	NP_001350521.1:p.Ile407=
NM_001363593.1:c.46A= (BEST1)	NP_001350522.1:p.Lys16=
NR_134580.1:n.1801A= (BEST1)
XM_005274210.4:c.1018A= (BEST1)	XP_005274267.1:p.Lys340=
XM_005274215.4:c.700A= (BEST1)	XP_005274272.1:p.Lys234=
XM_005274216.4:c.1041A= (BEST1)	XP_005274273.1:p.Ile347=
XM_005274219.4:c.867+1663A= (BEST1)	XP_005274276.1:n.867+1663A=
XM_005274221.4:c.715-2294A= (BEST1)	XP_005274278.1:n.715-2294A=
XM_011545229.3:c.1018A= (BEST1)	XP_011543531.1:p.Lys340=
XM_011545230.3:c.925A= (BEST1)	XP_011543532.1:p.Lys309=
XM_011545233.3:c.175A= (BEST1)	XP_011543535.1:p.Lys59=
XM_017018230.2:c.903A= (BEST1)	XP_016873719.1:p.Ile301=
XR_001747952.2:n.1719A= (BEST1)
XR_001747953.2:n.1557+1663A= (BEST1)
XR_001747954.2:n.1405-2294A= (BEST1)
NM_004183.4:c.1018A= (BEST1) MANE Select	NP_004174.1:p.Lys340=
NM_001139443.2:c.838A= (BEST1)	NP_001132915.1:p.Lys280=
NM_001300786.2:c.757A= (BEST1)	NP_001287715.1:p.Lys253=
NM_001300787.2:c.838A= (BEST1)	NP_001287716.1:p.Lys280=
NM_001363591.2:c.700A= (BEST1)	NP_001350520.1:p.Lys234=
NM_001363593.2:c.46A= (BEST1)	NP_001350522.1:p.Lys16=
NR_134580.2:n.1334A= (BEST1)