Canonical Allele Identifier: CA1977532038
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61958327G= , CM000673.2:g.61958327G= GRCh38
NC_000011.9:g.61725799G= , CM000673.1:g.61725799G= GRCh37
NC_000011.8:g.61482375G= NCBI36
NG_009033.1:g.13444G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.867+29G= MANE Select ENSP00000367282.4:n.867+29G=
ENST00000378043.8:c.867+29G= ENSP00000367282.4:n.867+29G=
ENST00000449131.6:c.687+29G= ENSP00000399709.2:n.687+29G=
ENST00000524877.5:n.1328G=
ENST00000524926.5:c.896G= ENSP00000432681.1:p.Trp299=
ENST00000526988.1:c.578G= ENSP00000433195.1:p.Trp193=
ENST00000529265.5:n.819G=
ENST00000534553.5:c.163+2376G= ENSP00000431189.1:n.163+2376G=
NM_001139443.1:c.687+29G= NP_001132915.1:n.687+29G=
NM_001300786.1:c.687+29G= NP_001287715.1:n.687+29G=
NM_001300787.1:c.687+29G= NP_001287716.1:n.687+29G=
NM_004183.3:c.867+29G= NP_004174.1:n.867+29G=
XM_005274210.2:c.867+29G= XP_005274267.1:n.867+29G=
XM_005274215.2:c.549+29G= XP_005274272.1:n.549+29G=
XM_005274216.2:c.716G= XP_005274273.1:p.Trp239=
XM_005274218.3:c.578G= XP_005274275.1:p.Trp193=
XM_005274219.2:c.867+29G= XP_005274276.1:n.867+29G=
XM_005274221.2:c.714+863G= XP_005274278.1:n.714+863G=
XM_011545229.1:c.867+29G= XP_011543531.1:n.867+29G=
XM_011545230.1:c.774+29G= XP_011543532.1:n.774+29G=
XM_011545231.1:c.549+29G= XP_011543533.1:n.549+29G=
XM_011545232.1:c.896G= XP_011543534.1:p.Trp299=
NM_001363591.1:c.549+29G= NP_001350520.1:n.549+29G=
NM_001363592.1:c.896G= NP_001350521.1:p.Trp299=
NM_001363593.1:c.-280G= NP_001350522.1:n.-280G=
NR_134580.1:n.1476G=
XM_005274210.4:c.867+29G= XP_005274267.1:n.867+29G=
XM_005274215.4:c.549+29G= XP_005274272.1:n.549+29G=
XM_005274216.4:c.716G= XP_005274273.1:p.Trp239=
XM_005274219.4:c.867+29G= XP_005274276.1:n.867+29G=
XM_005274221.4:c.714+863G= XP_005274278.1:n.714+863G=
XM_011545229.3:c.867+29G= XP_011543531.1:n.867+29G=
XM_011545230.3:c.774+29G= XP_011543532.1:n.774+29G=
XM_017018230.2:c.578G= XP_016873719.1:p.Trp193=
XR_001747952.2:n.1394G=
XR_001747953.2:n.1557+29G=
XR_001747954.2:n.1404+863G=
XR_001748245.1:n.402C=
XR_002957249.1:n.402C=
NM_004183.4:c.867+29G= MANE Select NP_004174.1:n.867+29G=
NM_001139443.2:c.687+29G= NP_001132915.1:n.687+29G=
NM_001300786.2:c.687+29G= NP_001287715.1:n.687+29G=
NM_001300787.2:c.687+29G= NP_001287716.1:n.687+29G=
NM_001363591.2:c.549+29G= NP_001350520.1:n.549+29G=
NM_001363593.2:c.-280G= NP_001350522.1:n.-280G=
NR_134580.2:n.1009G=