Canonical Allele Identifier: CA380833975
Gene: BEST1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61955732C>A , CM000673.2:g.61955732C>A GRCh38
NC_000011.9:g.61723204C>A , CM000673.1:g.61723204C>A GRCh37
NC_000011.8:g.61479780C>A NCBI36
NG_009033.1:g.10849C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.262C>A MANE Select ENSP00000367282.4:p.Leu88Met
ENST00000378043.8:c.262C>A ENSP00000367282.4:p.Leu88Met
ENST00000449131.6:c.82C>A ENSP00000399709.2:p.Leu28Met
ENST00000524877.5:n.694C>A
ENST00000524926.5:c.262C>A ENSP00000432681.1:p.Leu88Met
ENST00000526988.1:c.-57C>A ENSP00000433195.1:n.-57C>A
ENST00000529265.5:n.185C>A
ENST00000533521.5:n.886C>A
ENST00000534553.5:c.-57C>A ENSP00000431189.1:n.-57C>A
NM_001139443.1:c.82C>A NP_001132915.1:p.Leu28Met
NM_001300786.1:c.82C>A NP_001287715.1:p.Leu28Met
NM_001300787.1:c.82C>A NP_001287716.1:p.Leu28Met
NM_004183.3:c.262C>A NP_004174.1:p.Leu88Met
XM_005274210.2:c.262C>A XP_005274267.1:p.Leu88Met
XM_005274215.2:c.-57C>A XP_005274272.1:n.-57C>A
XM_005274216.2:c.82C>A XP_005274273.1:p.Leu28Met
XM_005274218.3:c.-57C>A XP_005274275.1:n.-57C>A
XM_005274219.2:c.262C>A XP_005274276.1:p.Leu88Met
XM_005274221.2:c.262C>A XP_005274278.1:p.Leu88Met
XM_011545229.1:c.262C>A XP_011543531.1:p.Leu88Met
XM_011545230.1:c.169C>A XP_011543532.1:p.Leu57Met
XM_011545231.1:c.-57C>A XP_011543533.1:n.-57C>A
XM_011545232.1:c.262C>A XP_011543534.1:p.Leu88Met
NM_001363591.1:c.-57C>A NP_001350520.1:n.-57C>A
NM_001363592.1:c.262C>A NP_001350521.1:p.Leu88Met
NM_001363593.1:c.-914C>A NP_001350522.1:n.-914C>A
NR_134580.1:n.842C>A
XM_005274210.4:c.262C>A XP_005274267.1:p.Leu88Met
XM_005274215.4:c.-57C>A XP_005274272.1:n.-57C>A
XM_005274216.4:c.82C>A XP_005274273.1:p.Leu28Met
XM_005274219.4:c.262C>A XP_005274276.1:p.Leu88Met
XM_005274221.4:c.262C>A XP_005274278.1:p.Leu88Met
XM_011545229.3:c.262C>A XP_011543531.1:p.Leu88Met
XM_011545230.3:c.169C>A XP_011543532.1:p.Leu57Met
XM_017018230.2:c.-57C>A XP_016873719.1:n.-57C>A
XR_001747952.2:n.760C>A
XR_001747953.2:n.952C>A
XR_001747954.2:n.952C>A
XR_002957249.1:n.2006G>T
NM_004183.4:c.262C>A MANE Select NP_004174.1:p.Leu88Met
NM_001139443.2:c.82C>A NP_001132915.1:p.Leu28Met
NM_001300786.2:c.82C>A NP_001287715.1:p.Leu28Met
NM_001300787.2:c.82C>A NP_001287716.1:p.Leu28Met
NM_001363591.2:c.-57C>A NP_001350520.1:n.-57C>A
NM_001363593.2:c.-914C>A NP_001350522.1:n.-914C>A
NR_134580.2:n.375C>A