Canonical Allele Identifier: CA1977534269
Gene: BEST1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959570A= , CM000673.2:g.61959570A= GRCh38
NC_000011.9:g.61727042A= , CM000673.1:g.61727042A= GRCh37
NC_000011.8:g.61483618A= NCBI36
NG_009033.1:g.14687A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.940A= MANE Select ENSP00000367282.4:p.Asn314=
ENST00000378043.8:c.940A= ENSP00000367282.4:p.Asn314=
ENST00000449131.6:c.760A= ENSP00000399709.2:p.Asn254=
ENST00000524877.5:n.2571A=
ENST00000524926.5:c.1143A= ENSP00000432681.1:p.Gly381=
ENST00000526988.1:c.825A= ENSP00000433195.1:p.Gly275=
ENST00000534553.5:c.164-2685A= ENSP00000431189.1:n.164-2685A=
NM_001139443.1:c.760A= NP_001132915.1:p.Asn254=
NM_001300786.1:c.688-322A= NP_001287715.1:n.688-322A=
NM_001300787.1:c.760A= NP_001287716.1:p.Asn254=
NM_004183.3:c.940A= NP_004174.1:p.Asn314=
XM_005274210.2:c.940A= XP_005274267.1:p.Asn314=
XM_005274215.2:c.622A= XP_005274272.1:p.Asn208=
XM_005274216.2:c.963A= XP_005274273.1:p.Gly321=
XM_005274218.3:c.825A= XP_005274275.1:p.Gly275=
XM_005274219.2:c.867+1272A= XP_005274276.1:n.867+1272A=
XM_005274221.2:c.714+2106A= XP_005274278.1:n.714+2106A=
XM_011545229.1:c.940A= XP_011543531.1:p.Asn314=
XM_011545230.1:c.847A= XP_011543532.1:p.Asn283=
XM_011545231.1:c.622A= XP_011543533.1:p.Asn208=
XM_011545232.1:c.1143A= XP_011543534.1:p.Gly381=
XM_011545233.1:c.97A= XP_011543535.1:p.Asn33=
NM_001363591.1:c.622A= NP_001350520.1:p.Asn208=
NM_001363592.1:c.1143A= NP_001350521.1:p.Gly381=
NM_001363593.1:c.-33A= NP_001350522.1:n.-33A=
NR_134580.1:n.1723A=
XM_005274210.4:c.940A= XP_005274267.1:p.Asn314=
XM_005274215.4:c.622A= XP_005274272.1:p.Asn208=
XM_005274216.4:c.963A= XP_005274273.1:p.Gly321=
XM_005274219.4:c.867+1272A= XP_005274276.1:n.867+1272A=
XM_005274221.4:c.714+2106A= XP_005274278.1:n.714+2106A=
XM_011545229.3:c.940A= XP_011543531.1:p.Asn314=
XM_011545230.3:c.847A= XP_011543532.1:p.Asn283=
XM_011545233.3:c.97A= XP_011543535.1:p.Asn33=
XM_017018230.2:c.825A= XP_016873719.1:p.Gly275=
XR_001747952.2:n.1641A=
XR_001747953.2:n.1557+1272A=
XR_001747954.2:n.1404+2106A=
XR_001748245.1:n.196+162T=
XR_002957249.1:n.196+162T=
NM_004183.4:c.940A= MANE Select NP_004174.1:p.Asn314=
NM_001139443.2:c.760A= NP_001132915.1:p.Asn254=
NM_001300786.2:c.688-322A= NP_001287715.1:n.688-322A=
NM_001300787.2:c.760A= NP_001287716.1:p.Asn254=
NM_001363591.2:c.622A= NP_001350520.1:p.Asn208=
NM_001363593.2:c.-33A= NP_001350522.1:n.-33A=
NR_134580.2:n.1256A=