Canonical Allele Identifier: CA380834447
Gene: BEST1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61955807T>C , CM000673.2:g.61955807T>C GRCh38
NC_000011.9:g.61723279T>C , CM000673.1:g.61723279T>C GRCh37
NC_000011.8:g.61479855T>C NCBI36
NG_009033.1:g.10924T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378043.9:c.337T>C MANE Select ENSP00000367282.4:p.Phe113Leu
ENST00000378043.8:c.337T>C ENSP00000367282.4:p.Phe113Leu
ENST00000449131.6:c.157T>C ENSP00000399709.2:p.Phe53Leu
ENST00000524877.5:n.769T>C
ENST00000524926.5:c.337T>C ENSP00000432681.1:p.Phe113Leu
ENST00000526988.1:c.19T>C ENSP00000433195.1:p.Phe7Leu
ENST00000529265.5:n.260T>C
ENST00000533521.5:n.961T>C
ENST00000534553.5:c.19T>C ENSP00000431189.1:p.Phe7Leu
NM_001139443.1:c.157T>C NP_001132915.1:p.Phe53Leu
NM_001300786.1:c.157T>C NP_001287715.1:p.Phe53Leu
NM_001300787.1:c.157T>C NP_001287716.1:p.Phe53Leu
NM_004183.3:c.337T>C NP_004174.1:p.Phe113Leu
XM_005274210.2:c.337T>C XP_005274267.1:p.Phe113Leu
XM_005274215.2:c.19T>C XP_005274272.1:p.Phe7Leu
XM_005274216.2:c.157T>C XP_005274273.1:p.Phe53Leu
XM_005274218.3:c.19T>C XP_005274275.1:p.Phe7Leu
XM_005274219.2:c.337T>C XP_005274276.1:p.Phe113Leu
XM_005274221.2:c.337T>C XP_005274278.1:p.Phe113Leu
XM_011545229.1:c.337T>C XP_011543531.1:p.Phe113Leu
XM_011545230.1:c.244T>C XP_011543532.1:p.Phe82Leu
XM_011545231.1:c.19T>C XP_011543533.1:p.Phe7Leu
XM_011545232.1:c.337T>C XP_011543534.1:p.Phe113Leu
NM_001363591.1:c.19T>C NP_001350520.1:p.Phe7Leu
NM_001363592.1:c.337T>C NP_001350521.1:p.Phe113Leu
NM_001363593.1:c.-839T>C NP_001350522.1:n.-839T>C
NR_134580.1:n.917T>C
XM_005274210.4:c.337T>C XP_005274267.1:p.Phe113Leu
XM_005274215.4:c.19T>C XP_005274272.1:p.Phe7Leu
XM_005274216.4:c.157T>C XP_005274273.1:p.Phe53Leu
XM_005274219.4:c.337T>C XP_005274276.1:p.Phe113Leu
XM_005274221.4:c.337T>C XP_005274278.1:p.Phe113Leu
XM_011545229.3:c.337T>C XP_011543531.1:p.Phe113Leu
XM_011545230.3:c.244T>C XP_011543532.1:p.Phe82Leu
XM_017018230.2:c.19T>C XP_016873719.1:p.Phe7Leu
XR_001747952.2:n.835T>C
XR_001747953.2:n.1027T>C
XR_001747954.2:n.1027T>C
XR_002957249.1:n.1931A>G
NM_004183.4:c.337T>C MANE Select NP_004174.1:p.Phe113Leu
NM_001139443.2:c.157T>C NP_001132915.1:p.Phe53Leu
NM_001300786.2:c.157T>C NP_001287715.1:p.Phe53Leu
NM_001300787.2:c.157T>C NP_001287716.1:p.Phe53Leu
NM_001363591.2:c.19T>C NP_001350520.1:p.Phe7Leu
NM_001363593.2:c.-839T>C NP_001350522.1:n.-839T>C
NR_134580.2:n.450T>C