Canonical Allele Identifier: CA380846107

Gene: BEST1 FTH1

Linked Data

• MyVariant Identifiers: chr11:g.61727392A>G (hg19) ; chr11:g.61959920A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959920A>G , CM000673.2:g.61959920A>G	GRCh38
NC_000011.9:g.61727392A>G , CM000673.1:g.61727392A>G	GRCh37
NC_000011.8:g.61483968A>G	NCBI36
NG_009033.1:g.15037A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.977A>G (BEST1) MANE Select	ENSP00000367282.4:p.His326Arg
ENST00000378043.8:c.977A>G (BEST1)	ENSP00000367282.4:p.His326Arg
ENST00000449131.6:c.797A>G (BEST1)	ENSP00000399709.2:p.His266Arg
ENST00000524877.5:n.2608A>G (BEST1)
ENST00000524926.5:c.1180A>G (BEST1)	ENSP00000432681.1:p.Thr394Ala
ENST00000526988.1:c.862A>G (BEST1)	ENSP00000433195.1:p.Thr288Ala
ENST00000529191.5:c.122T>C (FTH1)	ENSP00000431659.1:p.Val41Ala
ENST00000529631.5:c.115-16T>C (FTH1)	ENSP00000431575.1:n.115-16T>C
ENST00000530019.5:c.262-16T>C (FTH1)	ENSP00000433470.1:n.262-16T>C
ENST00000534553.5:c.164-2335A>G (BEST1)	ENSP00000431189.1:n.164-2335A>G
NM_001139443.1:c.797A>G (BEST1)	NP_001132915.1:p.His266Arg
NM_001300786.1:c.716A>G (BEST1)	NP_001287715.1:p.His239Arg
NM_001300787.1:c.797A>G (BEST1)	NP_001287716.1:p.His266Arg
NM_004183.3:c.977A>G (BEST1)	NP_004174.1:p.His326Arg
XM_005274210.2:c.977A>G (BEST1)	XP_005274267.1:p.His326Arg
XM_005274215.2:c.659A>G (BEST1)	XP_005274272.1:p.His220Arg
XM_005274216.2:c.1000A>G (BEST1)	XP_005274273.1:p.Thr334Ala
XM_005274218.3:c.862A>G (BEST1)	XP_005274275.1:p.Thr288Ala
XM_005274219.2:c.867+1622A>G (BEST1)	XP_005274276.1:n.867+1622A>G
XM_005274221.2:c.715-2335A>G (BEST1)	XP_005274278.1:n.715-2335A>G
XM_011545229.1:c.977A>G (BEST1)	XP_011543531.1:p.His326Arg
XM_011545230.1:c.884A>G (BEST1)	XP_011543532.1:p.His295Arg
XM_011545231.1:c.659A>G (BEST1)	XP_011543533.1:p.His220Arg
XM_011545232.1:c.1180A>G (BEST1)	XP_011543534.1:p.Thr394Ala
XM_011545233.1:c.134A>G (BEST1)	XP_011543535.1:p.His45Arg
NM_001363591.1:c.659A>G (BEST1)	NP_001350520.1:p.His220Arg
NM_001363592.1:c.1180A>G (BEST1)	NP_001350521.1:p.Thr394Ala
NM_001363593.1:c.5A>G (BEST1)	NP_001350522.1:p.His2Arg
NR_134580.1:n.1760A>G (BEST1)
XM_005274210.4:c.977A>G (BEST1)	XP_005274267.1:p.His326Arg
XM_005274215.4:c.659A>G (BEST1)	XP_005274272.1:p.His220Arg
XM_005274216.4:c.1000A>G (BEST1)	XP_005274273.1:p.Thr334Ala
XM_005274219.4:c.867+1622A>G (BEST1)	XP_005274276.1:n.867+1622A>G
XM_005274221.4:c.715-2335A>G (BEST1)	XP_005274278.1:n.715-2335A>G
XM_011545229.3:c.977A>G (BEST1)	XP_011543531.1:p.His326Arg
XM_011545230.3:c.884A>G (BEST1)	XP_011543532.1:p.His295Arg
XM_011545233.3:c.134A>G (BEST1)	XP_011543535.1:p.His45Arg
XM_017018230.2:c.862A>G (BEST1)	XP_016873719.1:p.Thr288Ala
XR_001747952.2:n.1678A>G (BEST1)
XR_001747953.2:n.1557+1622A>G (BEST1)
XR_001747954.2:n.1405-2335A>G (BEST1)
XR_001748245.1:n.8T>C
XR_002957249.1:n.8T>C
NM_004183.4:c.977A>G (BEST1) MANE Select	NP_004174.1:p.His326Arg
NM_001139443.2:c.797A>G (BEST1)	NP_001132915.1:p.His266Arg
NM_001300786.2:c.716A>G (BEST1)	NP_001287715.1:p.His239Arg
NM_001300787.2:c.797A>G (BEST1)	NP_001287716.1:p.His266Arg
NM_001363591.2:c.659A>G (BEST1)	NP_001350520.1:p.His220Arg
NM_001363593.2:c.5A>G (BEST1)	NP_001350522.1:p.His2Arg
NR_134580.2:n.1293A>G (BEST1)