Canonical Allele Identifier: CA1977531746
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61958195G= , CM000673.2:g.61958195G= GRCh38
NC_000011.9:g.61725667G= , CM000673.1:g.61725667G= GRCh37
NC_000011.8:g.61482243G= NCBI36
NG_009033.1:g.13312G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.764G= MANE Select ENSP00000367282.4:p.Arg255=
ENST00000378043.8:c.764G= ENSP00000367282.4:p.Arg255=
ENST00000449131.6:c.584G= ENSP00000399709.2:p.Arg195=
ENST00000524877.5:n.1196G=
ENST00000524926.5:c.764G= ENSP00000432681.1:p.Arg255=
ENST00000526988.1:c.446G= ENSP00000433195.1:p.Arg149=
ENST00000529265.5:n.687G=
ENST00000534553.5:c.163+2244G= ENSP00000431189.1:n.163+2244G=
NM_001139443.1:c.584G= NP_001132915.1:p.Arg195=
NM_001300786.1:c.584G= NP_001287715.1:p.Arg195=
NM_001300787.1:c.584G= NP_001287716.1:p.Arg195=
NM_004183.3:c.764G= NP_004174.1:p.Arg255=
XM_005274210.2:c.764G= XP_005274267.1:p.Arg255=
XM_005274215.2:c.446G= XP_005274272.1:p.Arg149=
XM_005274216.2:c.584G= XP_005274273.1:p.Arg195=
XM_005274218.3:c.446G= XP_005274275.1:p.Arg149=
XM_005274219.2:c.764G= XP_005274276.1:p.Arg255=
XM_005274221.2:c.714+731G= XP_005274278.1:n.714+731G=
XM_011545229.1:c.764G= XP_011543531.1:p.Arg255=
XM_011545230.1:c.671G= XP_011543532.1:p.Arg224=
XM_011545231.1:c.446G= XP_011543533.1:p.Arg149=
XM_011545232.1:c.764G= XP_011543534.1:p.Arg255=
NM_001363591.1:c.446G= NP_001350520.1:p.Arg149=
NM_001363592.1:c.764G= NP_001350521.1:p.Arg255=
NM_001363593.1:c.-412G= NP_001350522.1:n.-412G=
NR_134580.1:n.1344G=
XM_005274210.4:c.764G= XP_005274267.1:p.Arg255=
XM_005274215.4:c.446G= XP_005274272.1:p.Arg149=
XM_005274216.4:c.584G= XP_005274273.1:p.Arg195=
XM_005274219.4:c.764G= XP_005274276.1:p.Arg255=
XM_005274221.4:c.714+731G= XP_005274278.1:n.714+731G=
XM_011545229.3:c.764G= XP_011543531.1:p.Arg255=
XM_011545230.3:c.671G= XP_011543532.1:p.Arg224=
XM_017018230.2:c.446G= XP_016873719.1:p.Arg149=
XR_001747952.2:n.1262G=
XR_001747953.2:n.1454G=
XR_001747954.2:n.1404+731G=
XR_001748245.1:n.534C=
XR_002957249.1:n.505+29C=
NM_004183.4:c.764G= MANE Select NP_004174.1:p.Arg255=
NM_001139443.2:c.584G= NP_001132915.1:p.Arg195=
NM_001300786.2:c.584G= NP_001287715.1:p.Arg195=
NM_001300787.2:c.584G= NP_001287716.1:p.Arg195=
NM_001363591.2:c.446G= NP_001350520.1:p.Arg149=
NM_001363593.2:c.-412G= NP_001350522.1:n.-412G=
NR_134580.2:n.877G=