Canonical Allele Identifier: CA380846095

Gene: BEST1 FTH1

Linked Data

• COSMIC: COSM415501 ; COSM1133361
• MyVariant Identifiers: chr11:g.61727388A>G (hg19) ; chr11:g.61959916A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959916A>G , CM000673.2:g.61959916A>G	GRCh38
NC_000011.9:g.61727388A>G , CM000673.1:g.61727388A>G	GRCh37
NC_000011.8:g.61483964A>G	NCBI36
NG_009033.1:g.15033A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.973A>G (BEST1) MANE Select	ENSP00000367282.4:p.Met325Val
ENST00000378043.8:c.973A>G (BEST1)	ENSP00000367282.4:p.Met325Val
ENST00000449131.6:c.793A>G (BEST1)	ENSP00000399709.2:p.Met265Val
ENST00000524877.5:n.2604A>G (BEST1)
ENST00000524926.5:c.1176A>G (BEST1)	ENSP00000432681.1:p.Arg392=
ENST00000526988.1:c.858A>G (BEST1)	ENSP00000433195.1:p.Arg286=
ENST00000529191.5:c.126T>C (FTH1)	ENSP00000431659.1:p.His42=
ENST00000529631.5:c.115-12T>C (FTH1)	ENSP00000431575.1:n.115-12T>C
ENST00000530019.5:c.262-12T>C (FTH1)	ENSP00000433470.1:n.262-12T>C
ENST00000534553.5:c.164-2339A>G (BEST1)	ENSP00000431189.1:n.164-2339A>G
NM_001139443.1:c.793A>G (BEST1)	NP_001132915.1:p.Met265Val
NM_001300786.1:c.712A>G (BEST1)	NP_001287715.1:p.Met238Val
NM_001300787.1:c.793A>G (BEST1)	NP_001287716.1:p.Met265Val
NM_004183.3:c.973A>G (BEST1)	NP_004174.1:p.Met325Val
XM_005274210.2:c.973A>G (BEST1)	XP_005274267.1:p.Met325Val
XM_005274215.2:c.655A>G (BEST1)	XP_005274272.1:p.Met219Val
XM_005274216.2:c.996A>G (BEST1)	XP_005274273.1:p.Arg332=
XM_005274218.3:c.858A>G (BEST1)	XP_005274275.1:p.Arg286=
XM_005274219.2:c.867+1618A>G (BEST1)	XP_005274276.1:n.867+1618A>G
XM_005274221.2:c.715-2339A>G (BEST1)	XP_005274278.1:n.715-2339A>G
XM_011545229.1:c.973A>G (BEST1)	XP_011543531.1:p.Met325Val
XM_011545230.1:c.880A>G (BEST1)	XP_011543532.1:p.Met294Val
XM_011545231.1:c.655A>G (BEST1)	XP_011543533.1:p.Met219Val
XM_011545232.1:c.1176A>G (BEST1)	XP_011543534.1:p.Arg392=
XM_011545233.1:c.130A>G (BEST1)	XP_011543535.1:p.Met44Val
NM_001363591.1:c.655A>G (BEST1)	NP_001350520.1:p.Met219Val
NM_001363592.1:c.1176A>G (BEST1)	NP_001350521.1:p.Arg392=
NM_001363593.1:c.1A>G (BEST1)	NP_001350522.1:p.Met1Val
NR_134580.1:n.1756A>G (BEST1)
XM_005274210.4:c.973A>G (BEST1)	XP_005274267.1:p.Met325Val
XM_005274215.4:c.655A>G (BEST1)	XP_005274272.1:p.Met219Val
XM_005274216.4:c.996A>G (BEST1)	XP_005274273.1:p.Arg332=
XM_005274219.4:c.867+1618A>G (BEST1)	XP_005274276.1:n.867+1618A>G
XM_005274221.4:c.715-2339A>G (BEST1)	XP_005274278.1:n.715-2339A>G
XM_011545229.3:c.973A>G (BEST1)	XP_011543531.1:p.Met325Val
XM_011545230.3:c.880A>G (BEST1)	XP_011543532.1:p.Met294Val
XM_011545233.3:c.130A>G (BEST1)	XP_011543535.1:p.Met44Val
XM_017018230.2:c.858A>G (BEST1)	XP_016873719.1:p.Arg286=
XR_001747952.2:n.1674A>G (BEST1)
XR_001747953.2:n.1557+1618A>G (BEST1)
XR_001747954.2:n.1405-2339A>G (BEST1)
XR_001748245.1:n.12T>C
XR_002957249.1:n.12T>C
NM_004183.4:c.973A>G (BEST1) MANE Select	NP_004174.1:p.Met325Val
NM_001139443.2:c.793A>G (BEST1)	NP_001132915.1:p.Met265Val
NM_001300786.2:c.712A>G (BEST1)	NP_001287715.1:p.Met238Val
NM_001300787.2:c.793A>G (BEST1)	NP_001287716.1:p.Met265Val
NM_001363591.2:c.655A>G (BEST1)	NP_001350520.1:p.Met219Val
NM_001363593.2:c.1A>G (BEST1)	NP_001350522.1:p.Met1Val
NR_134580.2:n.1289A>G (BEST1)