Canonical Allele Identifier: CA1977534177
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959549A= , CM000673.2:g.61959549A= GRCh38
NC_000011.9:g.61727021A= , CM000673.1:g.61727021A= GRCh37
NC_000011.8:g.61483597A= NCBI36
NG_009033.1:g.14666A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.919A= MANE Select ENSP00000367282.4:p.Thr307=
ENST00000378043.8:c.919A= ENSP00000367282.4:p.Thr307=
ENST00000449131.6:c.739A= ENSP00000399709.2:p.Thr247=
ENST00000524877.5:n.2550A=
ENST00000524926.5:c.1122A= ENSP00000432681.1:p.Arg374=
ENST00000526988.1:c.804A= ENSP00000433195.1:p.Arg268=
ENST00000534553.5:c.164-2706A= ENSP00000431189.1:n.164-2706A=
NM_001139443.1:c.739A= NP_001132915.1:p.Thr247=
NM_001300786.1:c.688-343A= NP_001287715.1:n.688-343A=
NM_001300787.1:c.739A= NP_001287716.1:p.Thr247=
NM_004183.3:c.919A= NP_004174.1:p.Thr307=
XM_005274210.2:c.919A= XP_005274267.1:p.Thr307=
XM_005274215.2:c.601A= XP_005274272.1:p.Thr201=
XM_005274216.2:c.942A= XP_005274273.1:p.Arg314=
XM_005274218.3:c.804A= XP_005274275.1:p.Arg268=
XM_005274219.2:c.867+1251A= XP_005274276.1:n.867+1251A=
XM_005274221.2:c.714+2085A= XP_005274278.1:n.714+2085A=
XM_011545229.1:c.919A= XP_011543531.1:p.Thr307=
XM_011545230.1:c.826A= XP_011543532.1:p.Thr276=
XM_011545231.1:c.601A= XP_011543533.1:p.Thr201=
XM_011545232.1:c.1122A= XP_011543534.1:p.Arg374=
XM_011545233.1:c.76A= XP_011543535.1:p.Thr26=
NM_001363591.1:c.601A= NP_001350520.1:p.Thr201=
NM_001363592.1:c.1122A= NP_001350521.1:p.Arg374=
NM_001363593.1:c.-54A= NP_001350522.1:n.-54A=
NR_134580.1:n.1702A=
XM_005274210.4:c.919A= XP_005274267.1:p.Thr307=
XM_005274215.4:c.601A= XP_005274272.1:p.Thr201=
XM_005274216.4:c.942A= XP_005274273.1:p.Arg314=
XM_005274219.4:c.867+1251A= XP_005274276.1:n.867+1251A=
XM_005274221.4:c.714+2085A= XP_005274278.1:n.714+2085A=
XM_011545229.3:c.919A= XP_011543531.1:p.Thr307=
XM_011545230.3:c.826A= XP_011543532.1:p.Thr276=
XM_011545233.3:c.76A= XP_011543535.1:p.Thr26=
XM_017018230.2:c.804A= XP_016873719.1:p.Arg268=
XR_001747952.2:n.1620A=
XR_001747953.2:n.1557+1251A=
XR_001747954.2:n.1404+2085A=
XR_001748245.1:n.196+183T=
XR_002957249.1:n.196+183T=
NM_004183.4:c.919A= MANE Select NP_004174.1:p.Thr307=
NM_001139443.2:c.739A= NP_001132915.1:p.Thr247=
NM_001300786.2:c.688-343A= NP_001287715.1:n.688-343A=
NM_001300787.2:c.739A= NP_001287716.1:p.Thr247=
NM_001363591.2:c.601A= NP_001350520.1:p.Thr201=
NM_001363593.2:c.-54A= NP_001350522.1:n.-54A=
NR_134580.2:n.1235A=