Canonical Allele Identifier: CA1977534950

Gene: BEST1 FTH1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61960038C= , CM000673.2:g.61960038C=	GRCh38
NC_000011.9:g.61727510C= , CM000673.1:g.61727510C=	GRCh37
NC_000011.8:g.61484086C=	NCBI36
NG_009033.1:g.15155C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.1095C= (BEST1) MANE Select	ENSP00000367282.4:p.Asn365=
ENST00000378043.8:c.1095C= (BEST1)	ENSP00000367282.4:p.Asn365=
ENST00000449131.6:c.915C= (BEST1)	ENSP00000399709.2:p.Asn305=
ENST00000524877.5:n.2726C= (BEST1)
ENST00000524926.5:c.1298C= (BEST1)	ENSP00000432681.1:p.Thr433=
ENST00000526988.1:c.980C= (BEST1)	ENSP00000433195.1:p.Thr327=
ENST00000529191.5:c.115-111G= (FTH1)	ENSP00000431659.1:n.115-111G=
ENST00000529631.5:c.115-134G= (FTH1)	ENSP00000431575.1:n.115-134G=
ENST00000530019.5:c.262-134G= (FTH1)	ENSP00000433470.1:n.262-134G=
ENST00000534553.5:c.164-2217C= (BEST1)	ENSP00000431189.1:n.164-2217C=
NM_001139443.1:c.915C= (BEST1)	NP_001132915.1:p.Asn305=
NM_001300786.1:c.834C= (BEST1)	NP_001287715.1:p.Asn278=
NM_001300787.1:c.915C= (BEST1)	NP_001287716.1:p.Asn305=
NM_004183.3:c.1095C= (BEST1)	NP_004174.1:p.Asn365=
XM_005274210.2:c.1095C= (BEST1)	XP_005274267.1:p.Asn365=
XM_005274215.2:c.777C= (BEST1)	XP_005274272.1:p.Asn259=
XM_005274216.2:c.1118C= (BEST1)	XP_005274273.1:p.Thr373=
XM_005274218.3:c.980C= (BEST1)	XP_005274275.1:p.Thr327=
XM_005274219.2:c.867+1740C= (BEST1)	XP_005274276.1:n.867+1740C=
XM_005274221.2:c.715-2217C= (BEST1)	XP_005274278.1:n.715-2217C=
XM_011545229.1:c.1095C= (BEST1)	XP_011543531.1:p.Asn365=
XM_011545230.1:c.1002C= (BEST1)	XP_011543532.1:p.Asn334=
XM_011545231.1:c.777C= (BEST1)	XP_011543533.1:p.Asn259=
XM_011545232.1:c.1298C= (BEST1)	XP_011543534.1:p.Thr433=
XM_011545233.1:c.252C= (BEST1)	XP_011543535.1:p.Asn84=
NM_001363591.1:c.777C= (BEST1)	NP_001350520.1:p.Asn259=
NM_001363592.1:c.1298C= (BEST1)	NP_001350521.1:p.Thr433=
NM_001363593.1:c.123C= (BEST1)	NP_001350522.1:p.Asn41=
NR_134580.1:n.1878C= (BEST1)
XM_005274210.4:c.1095C= (BEST1)	XP_005274267.1:p.Asn365=
XM_005274215.4:c.777C= (BEST1)	XP_005274272.1:p.Asn259=
XM_005274216.4:c.1118C= (BEST1)	XP_005274273.1:p.Thr373=
XM_005274219.4:c.867+1740C= (BEST1)	XP_005274276.1:n.867+1740C=
XM_005274221.4:c.715-2217C= (BEST1)	XP_005274278.1:n.715-2217C=
XM_011545229.3:c.1095C= (BEST1)	XP_011543531.1:p.Asn365=
XM_011545230.3:c.1002C= (BEST1)	XP_011543532.1:p.Asn334=
XM_011545233.3:c.252C= (BEST1)	XP_011543535.1:p.Asn84=
XM_017018230.2:c.980C= (BEST1)	XP_016873719.1:p.Thr327=
XR_001747952.2:n.1796C= (BEST1)
XR_001747953.2:n.1557+1740C= (BEST1)
XR_001747954.2:n.1405-2217C= (BEST1)
NM_004183.4:c.1095C= (BEST1) MANE Select	NP_004174.1:p.Asn365=
NM_001139443.2:c.915C= (BEST1)	NP_001132915.1:p.Asn305=
NM_001300786.2:c.834C= (BEST1)	NP_001287715.1:p.Asn278=
NM_001300787.2:c.915C= (BEST1)	NP_001287716.1:p.Asn305=
NM_001363591.2:c.777C= (BEST1)	NP_001350520.1:p.Asn259=
NM_001363593.2:c.123C= (BEST1)	NP_001350522.1:p.Asn41=
NR_134580.2:n.1411C= (BEST1)