Canonical Allele Identifier: CA1977534148
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959544T= , CM000673.2:g.61959544T= GRCh38
NC_000011.9:g.61727016T= , CM000673.1:g.61727016T= GRCh37
NC_000011.8:g.61483592T= NCBI36
NG_009033.1:g.14661T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.914T= MANE Select ENSP00000367282.4:p.Phe305=
ENST00000378043.8:c.914T= ENSP00000367282.4:p.Phe305=
ENST00000449131.6:c.734T= ENSP00000399709.2:p.Phe245=
ENST00000524877.5:n.2545T=
ENST00000524926.5:c.1117T= ENSP00000432681.1:p.Leu373=
ENST00000526988.1:c.799T= ENSP00000433195.1:p.Leu267=
ENST00000534553.5:c.164-2711T= ENSP00000431189.1:n.164-2711T=
NM_001139443.1:c.734T= NP_001132915.1:p.Phe245=
NM_001300786.1:c.688-348T= NP_001287715.1:n.688-348T=
NM_001300787.1:c.734T= NP_001287716.1:p.Phe245=
NM_004183.3:c.914T= NP_004174.1:p.Phe305=
XM_005274210.2:c.914T= XP_005274267.1:p.Phe305=
XM_005274215.2:c.596T= XP_005274272.1:p.Phe199=
XM_005274216.2:c.937T= XP_005274273.1:p.Leu313=
XM_005274218.3:c.799T= XP_005274275.1:p.Leu267=
XM_005274219.2:c.867+1246T= XP_005274276.1:n.867+1246T=
XM_005274221.2:c.714+2080T= XP_005274278.1:n.714+2080T=
XM_011545229.1:c.914T= XP_011543531.1:p.Phe305=
XM_011545230.1:c.821T= XP_011543532.1:p.Phe274=
XM_011545231.1:c.596T= XP_011543533.1:p.Phe199=
XM_011545232.1:c.1117T= XP_011543534.1:p.Leu373=
XM_011545233.1:c.71T= XP_011543535.1:p.Phe24=
NM_001363591.1:c.596T= NP_001350520.1:p.Phe199=
NM_001363592.1:c.1117T= NP_001350521.1:p.Leu373=
NM_001363593.1:c.-59T= NP_001350522.1:n.-59T=
NR_134580.1:n.1697T=
XM_005274210.4:c.914T= XP_005274267.1:p.Phe305=
XM_005274215.4:c.596T= XP_005274272.1:p.Phe199=
XM_005274216.4:c.937T= XP_005274273.1:p.Leu313=
XM_005274219.4:c.867+1246T= XP_005274276.1:n.867+1246T=
XM_005274221.4:c.714+2080T= XP_005274278.1:n.714+2080T=
XM_011545229.3:c.914T= XP_011543531.1:p.Phe305=
XM_011545230.3:c.821T= XP_011543532.1:p.Phe274=
XM_011545233.3:c.71T= XP_011543535.1:p.Phe24=
XM_017018230.2:c.799T= XP_016873719.1:p.Leu267=
XR_001747952.2:n.1615T=
XR_001747953.2:n.1557+1246T=
XR_001747954.2:n.1404+2080T=
XR_001748245.1:n.196+188A=
XR_002957249.1:n.196+188A=
NM_004183.4:c.914T= MANE Select NP_004174.1:p.Phe305=
NM_001139443.2:c.734T= NP_001132915.1:p.Phe245=
NM_001300786.2:c.688-348T= NP_001287715.1:n.688-348T=
NM_001300787.2:c.734T= NP_001287716.1:p.Phe245=
NM_001363591.2:c.596T= NP_001350520.1:p.Phe199=
NM_001363593.2:c.-59T= NP_001350522.1:n.-59T=
NR_134580.2:n.1230T=