Canonical Allele Identifier: CA1977534556

Gene: BEST1 FTH1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959840G= , CM000673.2:g.61959840G=	GRCh38
NC_000011.9:g.61727312G= , CM000673.1:g.61727312G=	GRCh37
NC_000011.8:g.61483888G=	NCBI36
NG_009033.1:g.14957G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.949-52G= (BEST1) MANE Select	ENSP00000367282.4:n.949-52G=
ENST00000378043.8:c.949-52G= (BEST1)	ENSP00000367282.4:n.949-52G=
ENST00000449131.6:c.769-52G= (BEST1)	ENSP00000399709.2:n.769-52G=
ENST00000524877.5:n.2580-52G= (BEST1)
ENST00000524926.5:c.1152-52G= (BEST1)	ENSP00000432681.1:n.1152-52G=
ENST00000526988.1:c.834-52G= (BEST1)	ENSP00000433195.1:n.834-52G=
ENST00000529191.5:c.202C= (FTH1)	ENSP00000431659.1:p.Pro68=
ENST00000529631.5:c.179C= (FTH1)	ENSP00000431575.1:p.Thr60=
ENST00000530019.5:c.326C= (FTH1)	ENSP00000433470.1:p.Thr109=
ENST00000534553.5:c.164-2415G= (BEST1)	ENSP00000431189.1:n.164-2415G=
NM_001139443.1:c.769-52G= (BEST1)	NP_001132915.1:n.769-52G=
NM_001300786.1:c.688-52G= (BEST1)	NP_001287715.1:n.688-52G=
NM_001300787.1:c.769-52G= (BEST1)	NP_001287716.1:n.769-52G=
NM_004183.3:c.949-52G= (BEST1)	NP_004174.1:n.949-52G=
XM_005274210.2:c.949-52G= (BEST1)	XP_005274267.1:n.949-52G=
XM_005274215.2:c.631-52G= (BEST1)	XP_005274272.1:n.631-52G=
XM_005274216.2:c.972-52G= (BEST1)	XP_005274273.1:n.972-52G=
XM_005274218.3:c.834-52G= (BEST1)	XP_005274275.1:n.834-52G=
XM_005274219.2:c.867+1542G= (BEST1)	XP_005274276.1:n.867+1542G=
XM_005274221.2:c.714+2376G= (BEST1)	XP_005274278.1:n.714+2376G=
XM_011545229.1:c.949-52G= (BEST1)	XP_011543531.1:n.949-52G=
XM_011545230.1:c.856-52G= (BEST1)	XP_011543532.1:n.856-52G=
XM_011545231.1:c.631-52G= (BEST1)	XP_011543533.1:n.631-52G=
XM_011545232.1:c.1152-52G= (BEST1)	XP_011543534.1:n.1152-52G=
XM_011545233.1:c.106-52G= (BEST1)	XP_011543535.1:n.106-52G=
NM_001363591.1:c.631-52G= (BEST1)	NP_001350520.1:n.631-52G=
NM_001363592.1:c.1152-52G= (BEST1)	NP_001350521.1:n.1152-52G=
NM_001363593.1:c.-24-52G= (BEST1)	NP_001350522.1:n.-24-52G=
NR_134580.1:n.1732-52G= (BEST1)
XM_005274210.4:c.949-52G= (BEST1)	XP_005274267.1:n.949-52G=
XM_005274215.4:c.631-52G= (BEST1)	XP_005274272.1:n.631-52G=
XM_005274216.4:c.972-52G= (BEST1)	XP_005274273.1:n.972-52G=
XM_005274219.4:c.867+1542G= (BEST1)	XP_005274276.1:n.867+1542G=
XM_005274221.4:c.714+2376G= (BEST1)	XP_005274278.1:n.714+2376G=
XM_011545229.3:c.949-52G= (BEST1)	XP_011543531.1:n.949-52G=
XM_011545230.3:c.856-52G= (BEST1)	XP_011543532.1:n.856-52G=
XM_011545233.3:c.106-52G= (BEST1)	XP_011543535.1:n.106-52G=
XM_017018230.2:c.834-52G= (BEST1)	XP_016873719.1:n.834-52G=
XR_001747952.2:n.1650-52G= (BEST1)
XR_001747953.2:n.1557+1542G= (BEST1)
XR_001747954.2:n.1404+2376G= (BEST1)
XR_001748245.1:n.88C=
XR_002957249.1:n.88C=
NM_004183.4:c.949-52G= (BEST1) MANE Select	NP_004174.1:n.949-52G=
NM_001139443.2:c.769-52G= (BEST1)	NP_001132915.1:n.769-52G=
NM_001300786.2:c.688-52G= (BEST1)	NP_001287715.1:n.688-52G=
NM_001300787.2:c.769-52G= (BEST1)	NP_001287716.1:n.769-52G=
NM_001363591.2:c.631-52G= (BEST1)	NP_001350520.1:n.631-52G=
NM_001363593.2:c.-24-52G= (BEST1)	NP_001350522.1:n.-24-52G=
NR_134580.2:n.1265-52G= (BEST1)