Canonical Allele Identifier: CA1977560693
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61955148T= , CM000673.2:g.61955148T= GRCh38
NC_000011.9:g.61722620T= , CM000673.1:g.61722620T= GRCh37
NC_000011.8:g.61479196T= NCBI36
NG_009033.1:g.10265T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.194T= MANE Select ENSP00000367282.4:p.Leu65=
ENST00000378043.8:c.194T= ENSP00000367282.4:p.Leu65=
ENST00000449131.6:c.14T= ENSP00000399709.2:p.Leu5=
ENST00000524877.5:n.110T=
ENST00000524926.5:c.194T= ENSP00000432681.1:p.Leu65=
ENST00000529265.5:n.117T=
ENST00000533521.5:n.302T=
ENST00000534553.5:c.-170T= ENSP00000431189.1:n.-170T=
NM_001139443.1:c.14T= NP_001132915.1:p.Leu5=
NM_001300786.1:c.14T= NP_001287715.1:p.Leu5=
NM_001300787.1:c.14T= NP_001287716.1:p.Leu5=
NM_004183.3:c.194T= NP_004174.1:p.Leu65=
XM_005274210.2:c.194T= XP_005274267.1:p.Leu65=
XM_005274216.2:c.14T= XP_005274273.1:p.Leu5=
XM_005274218.3:c.-170T= XP_005274275.1:n.-170T=
XM_005274219.2:c.194T= XP_005274276.1:p.Leu65=
XM_005274221.2:c.194T= XP_005274278.1:p.Leu65=
XM_011545229.1:c.194T= XP_011543531.1:p.Leu65=
XM_011545230.1:c.101T= XP_011543532.1:p.Leu34=
XM_011545231.1:c.-170T= XP_011543533.1:n.-170T=
XM_011545232.1:c.194T= XP_011543534.1:p.Leu65=
NM_001363591.1:c.-311T= NP_001350520.1:n.-311T=
NM_001363592.1:c.194T= NP_001350521.1:p.Leu65=
NM_001363593.1:c.-1168T= NP_001350522.1:n.-1168T=
NR_134580.1:n.774T=
XM_005274210.4:c.194T= XP_005274267.1:p.Leu65=
XM_005274215.4:c.-311T= XP_005274272.1:n.-311T=
XM_005274216.4:c.14T= XP_005274273.1:p.Leu5=
XM_005274219.4:c.194T= XP_005274276.1:p.Leu65=
XM_005274221.4:c.194T= XP_005274278.1:p.Leu65=
XM_011545229.3:c.194T= XP_011543531.1:p.Leu65=
XM_011545230.3:c.101T= XP_011543532.1:p.Leu34=
XM_017018230.2:c.-311T= XP_016873719.1:n.-311T=
XR_001747952.2:n.692T=
XR_001747953.2:n.884T=
XR_001747954.2:n.884T=
XR_002957249.1:n.2590A=
NM_004183.4:c.194T= MANE Select NP_004174.1:p.Leu65=
NM_001139443.2:c.14T= NP_001132915.1:p.Leu5=
NM_001300786.2:c.14T= NP_001287715.1:p.Leu5=
NM_001300787.2:c.14T= NP_001287716.1:p.Leu5=
NR_134580.2:n.307T=