Canonical Allele Identifier: CA1977533737
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959340G= , CM000673.2:g.61959340G= GRCh38
NC_000011.9:g.61726812G= , CM000673.1:g.61726812G= GRCh37
NC_000011.8:g.61483388G= NCBI36
NG_009033.1:g.14457G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.868-158G= MANE Select ENSP00000367282.4:n.868-158G=
ENST00000378043.8:c.868-158G= ENSP00000367282.4:n.868-158G=
ENST00000449131.6:c.688-158G= ENSP00000399709.2:n.688-158G=
ENST00000524877.5:n.2341G=
ENST00000524926.5:c.1071-158G= ENSP00000432681.1:n.1071-158G=
ENST00000526988.1:c.753-158G= ENSP00000433195.1:n.753-158G=
ENST00000534553.5:c.164-2915G= ENSP00000431189.1:n.164-2915G=
NM_001139443.1:c.688-158G= NP_001132915.1:n.688-158G=
NM_001300786.1:c.688-552G= NP_001287715.1:n.688-552G=
NM_001300787.1:c.688-158G= NP_001287716.1:n.688-158G=
NM_004183.3:c.868-158G= NP_004174.1:n.868-158G=
XM_005274210.2:c.868-158G= XP_005274267.1:n.868-158G=
XM_005274215.2:c.550-158G= XP_005274272.1:n.550-158G=
XM_005274216.2:c.891-158G= XP_005274273.1:n.891-158G=
XM_005274218.3:c.753-158G= XP_005274275.1:n.753-158G=
XM_005274219.2:c.867+1042G= XP_005274276.1:n.867+1042G=
XM_005274221.2:c.714+1876G= XP_005274278.1:n.714+1876G=
XM_011545229.1:c.868-158G= XP_011543531.1:n.868-158G=
XM_011545230.1:c.775-158G= XP_011543532.1:n.775-158G=
XM_011545231.1:c.550-158G= XP_011543533.1:n.550-158G=
XM_011545232.1:c.1071-158G= XP_011543534.1:n.1071-158G=
XM_011545233.1:c.24+135G= XP_011543535.1:n.24+135G=
NM_001363591.1:c.550-158G= NP_001350520.1:n.550-158G=
NM_001363592.1:c.1071-158G= NP_001350521.1:n.1071-158G=
NM_001363593.1:c.-105-158G= NP_001350522.1:n.-105-158G=
NR_134580.1:n.1651-158G=
XM_005274210.4:c.868-158G= XP_005274267.1:n.868-158G=
XM_005274215.4:c.550-158G= XP_005274272.1:n.550-158G=
XM_005274216.4:c.891-158G= XP_005274273.1:n.891-158G=
XM_005274219.4:c.867+1042G= XP_005274276.1:n.867+1042G=
XM_005274221.4:c.714+1876G= XP_005274278.1:n.714+1876G=
XM_011545229.3:c.868-158G= XP_011543531.1:n.868-158G=
XM_011545230.3:c.775-158G= XP_011543532.1:n.775-158G=
XM_011545233.3:c.24+135G= XP_011543535.1:n.24+135G=
XM_017018230.2:c.753-158G= XP_016873719.1:n.753-158G=
XR_001747952.2:n.1569-158G=
XR_001747953.2:n.1557+1042G=
XR_001747954.2:n.1404+1876G=
XR_001748245.1:n.196+392C=
XR_002957249.1:n.196+392C=
NM_004183.4:c.868-158G= MANE Select NP_004174.1:n.868-158G=
NM_001139443.2:c.688-158G= NP_001132915.1:n.688-158G=
NM_001300786.2:c.688-552G= NP_001287715.1:n.688-552G=
NM_001300787.2:c.688-158G= NP_001287716.1:n.688-158G=
NM_001363591.2:c.550-158G= NP_001350520.1:n.550-158G=
NM_001363593.2:c.-105-158G= NP_001350522.1:n.-105-158G=
NR_134580.2:n.1184-158G=