Canonical Allele Identifier: CA1977531958
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61958291G= , CM000673.2:g.61958291G= GRCh38
NC_000011.9:g.61725763G= , CM000673.1:g.61725763G= GRCh37
NC_000011.8:g.61482339G= NCBI36
NG_009033.1:g.13408G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.860G= MANE Select ENSP00000367282.4:p.Trp287=
ENST00000378043.8:c.860G= ENSP00000367282.4:p.Trp287=
ENST00000449131.6:c.680G= ENSP00000399709.2:p.Trp227=
ENST00000524877.5:n.1292G=
ENST00000524926.5:c.860G= ENSP00000432681.1:p.Trp287=
ENST00000526988.1:c.542G= ENSP00000433195.1:p.Trp181=
ENST00000529265.5:n.783G=
ENST00000534553.5:c.163+2340G= ENSP00000431189.1:n.163+2340G=
NM_001139443.1:c.680G= NP_001132915.1:p.Trp227=
NM_001300786.1:c.680G= NP_001287715.1:p.Trp227=
NM_001300787.1:c.680G= NP_001287716.1:p.Trp227=
NM_004183.3:c.860G= NP_004174.1:p.Trp287=
XM_005274210.2:c.860G= XP_005274267.1:p.Trp287=
XM_005274215.2:c.542G= XP_005274272.1:p.Trp181=
XM_005274216.2:c.680G= XP_005274273.1:p.Trp227=
XM_005274218.3:c.542G= XP_005274275.1:p.Trp181=
XM_005274219.2:c.860G= XP_005274276.1:p.Trp287=
XM_005274221.2:c.714+827G= XP_005274278.1:n.714+827G=
XM_011545229.1:c.860G= XP_011543531.1:p.Trp287=
XM_011545230.1:c.767G= XP_011543532.1:p.Trp256=
XM_011545231.1:c.542G= XP_011543533.1:p.Trp181=
XM_011545232.1:c.860G= XP_011543534.1:p.Trp287=
NM_001363591.1:c.542G= NP_001350520.1:p.Trp181=
NM_001363592.1:c.860G= NP_001350521.1:p.Trp287=
NM_001363593.1:c.-316G= NP_001350522.1:n.-316G=
NR_134580.1:n.1440G=
XM_005274210.4:c.860G= XP_005274267.1:p.Trp287=
XM_005274215.4:c.542G= XP_005274272.1:p.Trp181=
XM_005274216.4:c.680G= XP_005274273.1:p.Trp227=
XM_005274219.4:c.860G= XP_005274276.1:p.Trp287=
XM_005274221.4:c.714+827G= XP_005274278.1:n.714+827G=
XM_011545229.3:c.860G= XP_011543531.1:p.Trp287=
XM_011545230.3:c.767G= XP_011543532.1:p.Trp256=
XM_017018230.2:c.542G= XP_016873719.1:p.Trp181=
XR_001747952.2:n.1358G=
XR_001747953.2:n.1550G=
XR_001747954.2:n.1404+827G=
XR_001748245.1:n.438C=
XR_002957249.1:n.438C=
NM_004183.4:c.860G= MANE Select NP_004174.1:p.Trp287=
NM_001139443.2:c.680G= NP_001132915.1:p.Trp227=
NM_001300786.2:c.680G= NP_001287715.1:p.Trp227=
NM_001300787.2:c.680G= NP_001287716.1:p.Trp227=
NM_001363591.2:c.542G= NP_001350520.1:p.Trp181=
NM_001363593.2:c.-316G= NP_001350522.1:n.-316G=
NR_134580.2:n.973G=