Canonical Allele Identifier: CA1977533940
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959515C= , CM000673.2:g.61959515C= GRCh38
NC_000011.9:g.61726987C= , CM000673.1:g.61726987C= GRCh37
NC_000011.8:g.61483563C= NCBI36
NG_009033.1:g.14632C=

Transcript Alleles

HGVS Amino-acid change
ENST00000378043.9:c.885C= MANE Select ENSP00000367282.4:p.Ile295=
ENST00000378043.8:c.885C= ENSP00000367282.4:p.Ile295=
ENST00000449131.6:c.705C= ENSP00000399709.2:p.Ile235=
ENST00000524877.5:n.2516C=
ENST00000524926.5:c.1088C= ENSP00000432681.1:p.Ser363=
ENST00000526988.1:c.770C= ENSP00000433195.1:p.Ser257=
ENST00000534553.5:c.164-2740C= ENSP00000431189.1:n.164-2740C=
NM_001139443.1:c.705C= NP_001132915.1:p.Ile235=
NM_001300786.1:c.688-377C= NP_001287715.1:n.688-377C=
NM_001300787.1:c.705C= NP_001287716.1:p.Ile235=
NM_004183.3:c.885C= NP_004174.1:p.Ile295=
XM_005274210.2:c.885C= XP_005274267.1:p.Ile295=
XM_005274215.2:c.567C= XP_005274272.1:p.Ile189=
XM_005274216.2:c.908C= XP_005274273.1:p.Ser303=
XM_005274218.3:c.770C= XP_005274275.1:p.Ser257=
XM_005274219.2:c.867+1217C= XP_005274276.1:n.867+1217C=
XM_005274221.2:c.714+2051C= XP_005274278.1:n.714+2051C=
XM_011545229.1:c.885C= XP_011543531.1:p.Ile295=
XM_011545230.1:c.792C= XP_011543532.1:p.Ile264=
XM_011545231.1:c.567C= XP_011543533.1:p.Ile189=
XM_011545232.1:c.1088C= XP_011543534.1:p.Ser363=
XM_011545233.1:c.42C= XP_011543535.1:p.Ile14=
NM_001363591.1:c.567C= NP_001350520.1:p.Ile189=
NM_001363592.1:c.1088C= NP_001350521.1:p.Ser363=
NM_001363593.1:c.-88C= NP_001350522.1:n.-88C=
NR_134580.1:n.1668C=
XM_005274210.4:c.885C= XP_005274267.1:p.Ile295=
XM_005274215.4:c.567C= XP_005274272.1:p.Ile189=
XM_005274216.4:c.908C= XP_005274273.1:p.Ser303=
XM_005274219.4:c.867+1217C= XP_005274276.1:n.867+1217C=
XM_005274221.4:c.714+2051C= XP_005274278.1:n.714+2051C=
XM_011545229.3:c.885C= XP_011543531.1:p.Ile295=
XM_011545230.3:c.792C= XP_011543532.1:p.Ile264=
XM_011545233.3:c.42C= XP_011543535.1:p.Ile14=
XM_017018230.2:c.770C= XP_016873719.1:p.Ser257=
XR_001747952.2:n.1586C=
XR_001747953.2:n.1557+1217C=
XR_001747954.2:n.1404+2051C=
XR_001748245.1:n.196+217G=
XR_002957249.1:n.196+217G=
NM_004183.4:c.885C= MANE Select NP_004174.1:p.Ile295=
NM_001139443.2:c.705C= NP_001132915.1:p.Ile235=
NM_001300786.2:c.688-377C= NP_001287715.1:n.688-377C=
NM_001300787.2:c.705C= NP_001287716.1:p.Ile235=
NM_001363591.2:c.567C= NP_001350520.1:p.Ile189=
NM_001363593.2:c.-88C= NP_001350522.1:n.-88C=
NR_134580.2:n.1201C=