Canonical Allele Identifier: CA1977534276
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959576C= , CM000673.2:g.61959576C= GRCh38
NC_000011.9:g.61727048C= , CM000673.1:g.61727048C= GRCh37
NC_000011.8:g.61483624C= NCBI36
NG_009033.1:g.14693C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.946C= MANE Select ENSP00000367282.4:p.Gln316=
ENST00000378043.8:c.946C= ENSP00000367282.4:p.Gln316=
ENST00000449131.6:c.766C= ENSP00000399709.2:p.Gln256=
ENST00000524877.5:n.2577C=
ENST00000524926.5:c.1149C= ENSP00000432681.1:p.Cys383=
ENST00000526988.1:c.831C= ENSP00000433195.1:p.Cys277=
ENST00000534553.5:c.164-2679C= ENSP00000431189.1:n.164-2679C=
NM_001139443.1:c.766C= NP_001132915.1:p.Gln256=
NM_001300786.1:c.688-316C= NP_001287715.1:n.688-316C=
NM_001300787.1:c.766C= NP_001287716.1:p.Gln256=
NM_004183.3:c.946C= NP_004174.1:p.Gln316=
XM_005274210.2:c.946C= XP_005274267.1:p.Gln316=
XM_005274215.2:c.628C= XP_005274272.1:p.Gln210=
XM_005274216.2:c.969C= XP_005274273.1:p.Cys323=
XM_005274218.3:c.831C= XP_005274275.1:p.Cys277=
XM_005274219.2:c.867+1278C= XP_005274276.1:n.867+1278C=
XM_005274221.2:c.714+2112C= XP_005274278.1:n.714+2112C=
XM_011545229.1:c.946C= XP_011543531.1:p.Gln316=
XM_011545230.1:c.853C= XP_011543532.1:p.Gln285=
XM_011545231.1:c.628C= XP_011543533.1:p.Gln210=
XM_011545232.1:c.1149C= XP_011543534.1:p.Cys383=
XM_011545233.1:c.103C= XP_011543535.1:p.Gln35=
NM_001363591.1:c.628C= NP_001350520.1:p.Gln210=
NM_001363592.1:c.1149C= NP_001350521.1:p.Cys383=
NM_001363593.1:c.-27C= NP_001350522.1:n.-27C=
NR_134580.1:n.1729C=
XM_005274210.4:c.946C= XP_005274267.1:p.Gln316=
XM_005274215.4:c.628C= XP_005274272.1:p.Gln210=
XM_005274216.4:c.969C= XP_005274273.1:p.Cys323=
XM_005274219.4:c.867+1278C= XP_005274276.1:n.867+1278C=
XM_005274221.4:c.714+2112C= XP_005274278.1:n.714+2112C=
XM_011545229.3:c.946C= XP_011543531.1:p.Gln316=
XM_011545230.3:c.853C= XP_011543532.1:p.Gln285=
XM_011545233.3:c.103C= XP_011543535.1:p.Gln35=
XM_017018230.2:c.831C= XP_016873719.1:p.Cys277=
XR_001747952.2:n.1647C=
XR_001747953.2:n.1557+1278C=
XR_001747954.2:n.1404+2112C=
XR_001748245.1:n.196+156G=
XR_002957249.1:n.196+156G=
NM_004183.4:c.946C= MANE Select NP_004174.1:p.Gln316=
NM_001139443.2:c.766C= NP_001132915.1:p.Gln256=
NM_001300786.2:c.688-316C= NP_001287715.1:n.688-316C=
NM_001300787.2:c.766C= NP_001287716.1:p.Gln256=
NM_001363591.2:c.628C= NP_001350520.1:p.Gln210=
NM_001363593.2:c.-27C= NP_001350522.1:n.-27C=
NR_134580.2:n.1262C=