Canonical Allele Identifier: CA1977533905
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959504G= , CM000673.2:g.61959504G= GRCh38
NC_000011.9:g.61726976G= , CM000673.1:g.61726976G= GRCh37
NC_000011.8:g.61483552G= NCBI36
NG_009033.1:g.14621G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.874G= MANE Select ENSP00000367282.4:p.Glu292=
ENST00000378043.8:c.874G= ENSP00000367282.4:p.Glu292=
ENST00000449131.6:c.694G= ENSP00000399709.2:p.Glu232=
ENST00000524877.5:n.2505G=
ENST00000524926.5:c.1077G= ENSP00000432681.1:p.Gln359=
ENST00000526988.1:c.759G= ENSP00000433195.1:p.Gln253=
ENST00000534553.5:c.164-2751G= ENSP00000431189.1:n.164-2751G=
NM_001139443.1:c.694G= NP_001132915.1:p.Glu232=
NM_001300786.1:c.688-388G= NP_001287715.1:n.688-388G=
NM_001300787.1:c.694G= NP_001287716.1:p.Glu232=
NM_004183.3:c.874G= NP_004174.1:p.Glu292=
XM_005274210.2:c.874G= XP_005274267.1:p.Glu292=
XM_005274215.2:c.556G= XP_005274272.1:p.Glu186=
XM_005274216.2:c.897G= XP_005274273.1:p.Gln299=
XM_005274218.3:c.759G= XP_005274275.1:p.Gln253=
XM_005274219.2:c.867+1206G= XP_005274276.1:n.867+1206G=
XM_005274221.2:c.714+2040G= XP_005274278.1:n.714+2040G=
XM_011545229.1:c.874G= XP_011543531.1:p.Glu292=
XM_011545230.1:c.781G= XP_011543532.1:p.Glu261=
XM_011545231.1:c.556G= XP_011543533.1:p.Glu186=
XM_011545232.1:c.1077G= XP_011543534.1:p.Gln359=
XM_011545233.1:c.31G= XP_011543535.1:p.Glu11=
NM_001363591.1:c.556G= NP_001350520.1:p.Glu186=
NM_001363592.1:c.1077G= NP_001350521.1:p.Gln359=
NM_001363593.1:c.-99G= NP_001350522.1:n.-99G=
NR_134580.1:n.1657G=
XM_005274210.4:c.874G= XP_005274267.1:p.Glu292=
XM_005274215.4:c.556G= XP_005274272.1:p.Glu186=
XM_005274216.4:c.897G= XP_005274273.1:p.Gln299=
XM_005274219.4:c.867+1206G= XP_005274276.1:n.867+1206G=
XM_005274221.4:c.714+2040G= XP_005274278.1:n.714+2040G=
XM_011545229.3:c.874G= XP_011543531.1:p.Glu292=
XM_011545230.3:c.781G= XP_011543532.1:p.Glu261=
XM_011545233.3:c.31G= XP_011543535.1:p.Glu11=
XM_017018230.2:c.759G= XP_016873719.1:p.Gln253=
XR_001747952.2:n.1575G=
XR_001747953.2:n.1557+1206G=
XR_001747954.2:n.1404+2040G=
XR_001748245.1:n.196+228C=
XR_002957249.1:n.196+228C=
NM_004183.4:c.874G= MANE Select NP_004174.1:p.Glu292=
NM_001139443.2:c.694G= NP_001132915.1:p.Glu232=
NM_001300786.2:c.688-388G= NP_001287715.1:n.688-388G=
NM_001300787.2:c.694G= NP_001287716.1:p.Glu232=
NM_001363591.2:c.556G= NP_001350520.1:p.Glu186=
NM_001363593.2:c.-99G= NP_001350522.1:n.-99G=
NR_134580.2:n.1190G=