Canonical Allele Identifier: CA1977534001
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959519C= , CM000673.2:g.61959519C= GRCh38
NC_000011.9:g.61726991C= , CM000673.1:g.61726991C= GRCh37
NC_000011.8:g.61483567C= NCBI36
NG_009033.1:g.14636C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.889C= MANE Select ENSP00000367282.4:p.Pro297=
ENST00000378043.8:c.889C= ENSP00000367282.4:p.Pro297=
ENST00000449131.6:c.709C= ENSP00000399709.2:p.Pro237=
ENST00000524877.5:n.2520C=
ENST00000524926.5:c.1092C= ENSP00000432681.1:p.Thr364=
ENST00000526988.1:c.774C= ENSP00000433195.1:p.Thr258=
ENST00000534553.5:c.164-2736C= ENSP00000431189.1:n.164-2736C=
NM_001139443.1:c.709C= NP_001132915.1:p.Pro237=
NM_001300786.1:c.688-373C= NP_001287715.1:n.688-373C=
NM_001300787.1:c.709C= NP_001287716.1:p.Pro237=
NM_004183.3:c.889C= NP_004174.1:p.Pro297=
XM_005274210.2:c.889C= XP_005274267.1:p.Pro297=
XM_005274215.2:c.571C= XP_005274272.1:p.Pro191=
XM_005274216.2:c.912C= XP_005274273.1:p.Thr304=
XM_005274218.3:c.774C= XP_005274275.1:p.Thr258=
XM_005274219.2:c.867+1221C= XP_005274276.1:n.867+1221C=
XM_005274221.2:c.714+2055C= XP_005274278.1:n.714+2055C=
XM_011545229.1:c.889C= XP_011543531.1:p.Pro297=
XM_011545230.1:c.796C= XP_011543532.1:p.Pro266=
XM_011545231.1:c.571C= XP_011543533.1:p.Pro191=
XM_011545232.1:c.1092C= XP_011543534.1:p.Thr364=
XM_011545233.1:c.46C= XP_011543535.1:p.Pro16=
NM_001363591.1:c.571C= NP_001350520.1:p.Pro191=
NM_001363592.1:c.1092C= NP_001350521.1:p.Thr364=
NM_001363593.1:c.-84C= NP_001350522.1:n.-84C=
NR_134580.1:n.1672C=
XM_005274210.4:c.889C= XP_005274267.1:p.Pro297=
XM_005274215.4:c.571C= XP_005274272.1:p.Pro191=
XM_005274216.4:c.912C= XP_005274273.1:p.Thr304=
XM_005274219.4:c.867+1221C= XP_005274276.1:n.867+1221C=
XM_005274221.4:c.714+2055C= XP_005274278.1:n.714+2055C=
XM_011545229.3:c.889C= XP_011543531.1:p.Pro297=
XM_011545230.3:c.796C= XP_011543532.1:p.Pro266=
XM_011545233.3:c.46C= XP_011543535.1:p.Pro16=
XM_017018230.2:c.774C= XP_016873719.1:p.Thr258=
XR_001747952.2:n.1590C=
XR_001747953.2:n.1557+1221C=
XR_001747954.2:n.1404+2055C=
XR_001748245.1:n.196+213G=
XR_002957249.1:n.196+213G=
NM_004183.4:c.889C= MANE Select NP_004174.1:p.Pro297=
NM_001139443.2:c.709C= NP_001132915.1:p.Pro237=
NM_001300786.2:c.688-373C= NP_001287715.1:n.688-373C=
NM_001300787.2:c.709C= NP_001287716.1:p.Pro237=
NM_001363591.2:c.571C= NP_001350520.1:p.Pro191=
NM_001363593.2:c.-84C= NP_001350522.1:n.-84C=
NR_134580.2:n.1205C=