Canonical Allele Identifier: CA1977534038
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959528G= , CM000673.2:g.61959528G= GRCh38
NC_000011.9:g.61727000G= , CM000673.1:g.61727000G= GRCh37
NC_000011.8:g.61483576G= NCBI36
NG_009033.1:g.14645G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.898G= MANE Select ENSP00000367282.4:p.Glu300=
ENST00000378043.8:c.898G= ENSP00000367282.4:p.Glu300=
ENST00000449131.6:c.718G= ENSP00000399709.2:p.Glu240=
ENST00000524877.5:n.2529G=
ENST00000524926.5:c.1101G= ENSP00000432681.1:p.Glu367=
ENST00000526988.1:c.783G= ENSP00000433195.1:p.Glu261=
ENST00000534553.5:c.164-2727G= ENSP00000431189.1:n.164-2727G=
NM_001139443.1:c.718G= NP_001132915.1:p.Glu240=
NM_001300786.1:c.688-364G= NP_001287715.1:n.688-364G=
NM_001300787.1:c.718G= NP_001287716.1:p.Glu240=
NM_004183.3:c.898G= NP_004174.1:p.Glu300=
XM_005274210.2:c.898G= XP_005274267.1:p.Glu300=
XM_005274215.2:c.580G= XP_005274272.1:p.Glu194=
XM_005274216.2:c.921G= XP_005274273.1:p.Glu307=
XM_005274218.3:c.783G= XP_005274275.1:p.Glu261=
XM_005274219.2:c.867+1230G= XP_005274276.1:n.867+1230G=
XM_005274221.2:c.714+2064G= XP_005274278.1:n.714+2064G=
XM_011545229.1:c.898G= XP_011543531.1:p.Glu300=
XM_011545230.1:c.805G= XP_011543532.1:p.Glu269=
XM_011545231.1:c.580G= XP_011543533.1:p.Glu194=
XM_011545232.1:c.1101G= XP_011543534.1:p.Glu367=
XM_011545233.1:c.55G= XP_011543535.1:p.Glu19=
NM_001363591.1:c.580G= NP_001350520.1:p.Glu194=
NM_001363592.1:c.1101G= NP_001350521.1:p.Glu367=
NM_001363593.1:c.-75G= NP_001350522.1:n.-75G=
NR_134580.1:n.1681G=
XM_005274210.4:c.898G= XP_005274267.1:p.Glu300=
XM_005274215.4:c.580G= XP_005274272.1:p.Glu194=
XM_005274216.4:c.921G= XP_005274273.1:p.Glu307=
XM_005274219.4:c.867+1230G= XP_005274276.1:n.867+1230G=
XM_005274221.4:c.714+2064G= XP_005274278.1:n.714+2064G=
XM_011545229.3:c.898G= XP_011543531.1:p.Glu300=
XM_011545230.3:c.805G= XP_011543532.1:p.Glu269=
XM_011545233.3:c.55G= XP_011543535.1:p.Glu19=
XM_017018230.2:c.783G= XP_016873719.1:p.Glu261=
XR_001747952.2:n.1599G=
XR_001747953.2:n.1557+1230G=
XR_001747954.2:n.1404+2064G=
XR_001748245.1:n.196+204C=
XR_002957249.1:n.196+204C=
NM_004183.4:c.898G= MANE Select NP_004174.1:p.Glu300=
NM_001139443.2:c.718G= NP_001132915.1:p.Glu240=
NM_001300786.2:c.688-364G= NP_001287715.1:n.688-364G=
NM_001300787.2:c.718G= NP_001287716.1:p.Glu240=
NM_001363591.2:c.580G= NP_001350520.1:p.Glu194=
NM_001363593.2:c.-75G= NP_001350522.1:n.-75G=
NR_134580.2:n.1214G=