Canonical Allele Identifier: CA1977560668
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61955109T= , CM000673.2:g.61955109T= GRCh38
NC_000011.9:g.61722581T= , CM000673.1:g.61722581T= GRCh37
NC_000011.8:g.61479157T= NCBI36
NG_009033.1:g.10226T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.155T= MANE Select ENSP00000367282.4:p.Leu52=
ENST00000378043.8:c.155T= ENSP00000367282.4:p.Leu52=
ENST00000449131.6:c.-26T= ENSP00000399709.2:n.-26T=
ENST00000524877.5:n.71T=
ENST00000524926.5:c.155T= ENSP00000432681.1:p.Leu52=
ENST00000529265.5:n.78T=
ENST00000533521.5:n.263T=
ENST00000534553.5:c.-209T= ENSP00000431189.1:n.-209T=
NM_001139443.1:c.-26T= NP_001132915.1:n.-26T=
NM_001300786.1:c.-26T= NP_001287715.1:n.-26T=
NM_001300787.1:c.-26T= NP_001287716.1:n.-26T=
NM_004183.3:c.155T= NP_004174.1:p.Leu52=
XM_005274210.2:c.155T= XP_005274267.1:p.Leu52=
XM_005274216.2:c.-26T= XP_005274273.1:n.-26T=
XM_005274218.3:c.-209T= XP_005274275.1:n.-209T=
XM_005274219.2:c.155T= XP_005274276.1:p.Leu52=
XM_005274221.2:c.155T= XP_005274278.1:p.Leu52=
XM_011545229.1:c.155T= XP_011543531.1:p.Leu52=
XM_011545230.1:c.62T= XP_011543532.1:p.Leu21=
XM_011545231.1:c.-209T= XP_011543533.1:n.-209T=
XM_011545232.1:c.155T= XP_011543534.1:p.Leu52=
NM_001363591.1:c.-350T= NP_001350520.1:n.-350T=
NM_001363592.1:c.155T= NP_001350521.1:p.Leu52=
NM_001363593.1:c.-1207T= NP_001350522.1:n.-1207T=
NR_134580.1:n.735T=
XM_005274210.4:c.155T= XP_005274267.1:p.Leu52=
XM_005274215.4:c.-350T= XP_005274272.1:n.-350T=
XM_005274216.4:c.-26T= XP_005274273.1:n.-26T=
XM_005274219.4:c.155T= XP_005274276.1:p.Leu52=
XM_005274221.4:c.155T= XP_005274278.1:p.Leu52=
XM_011545229.3:c.155T= XP_011543531.1:p.Leu52=
XM_011545230.3:c.62T= XP_011543532.1:p.Leu21=
XM_017018230.2:c.-350T= XP_016873719.1:n.-350T=
XR_001747952.2:n.653T=
XR_001747953.2:n.845T=
XR_001747954.2:n.845T=
XR_002957249.1:n.2629A=
NM_004183.4:c.155T= MANE Select NP_004174.1:p.Leu52=
NM_001139443.2:c.-26T= NP_001132915.1:n.-26T=
NM_001300786.2:c.-26T= NP_001287715.1:n.-26T=
NM_001300787.2:c.-26T= NP_001287716.1:n.-26T=
NR_134580.2:n.268T=