Canonical Allele Identifier: CA380838932

Gene: BEST1

Linked Data

• ClinVar Variation Id: 1457853
• ClinVar RCV Id: RCV001972730
• dbSNP Id: rs2134440586
• MyVariant Identifiers: chr11:g.61724931A>T (hg19) ; chr11:g.61957459A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61957459A>T , CM000673.2:g.61957459A>T	GRCh38
NC_000011.9:g.61724931A>T , CM000673.1:g.61724931A>T	GRCh37
NC_000011.8:g.61481507A>T	NCBI36
NG_009033.1:g.12576A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378043.9:c.709A>T MANE Select	ENSP00000367282.4:p.Thr237Ser
ENST00000378043.8:c.709A>T	ENSP00000367282.4:p.Thr237Ser
ENST00000449131.6:c.529A>T	ENSP00000399709.2:p.Thr177Ser
ENST00000524877.5:n.1141A>T
ENST00000524926.5:c.709A>T	ENSP00000432681.1:p.Thr237Ser
ENST00000526988.1:c.391A>T	ENSP00000433195.1:p.Thr131Ser
ENST00000529265.5:n.632A>T
ENST00000534553.5:c.163+1508A>T	ENSP00000431189.1:n.163+1508A>T
NM_001139443.1:c.529A>T	NP_001132915.1:p.Thr177Ser
NM_001300786.1:c.529A>T	NP_001287715.1:p.Thr177Ser
NM_001300787.1:c.529A>T	NP_001287716.1:p.Thr177Ser
NM_004183.3:c.709A>T	NP_004174.1:p.Thr237Ser
XM_005274210.2:c.709A>T	XP_005274267.1:p.Thr237Ser
XM_005274215.2:c.391A>T	XP_005274272.1:p.Thr131Ser
XM_005274216.2:c.529A>T	XP_005274273.1:p.Thr177Ser
XM_005274218.3:c.391A>T	XP_005274275.1:p.Thr131Ser
XM_005274219.2:c.709A>T	XP_005274276.1:p.Thr237Ser
XM_005274221.2:c.709A>T	XP_005274278.1:p.Thr237Ser
XM_011545229.1:c.709A>T	XP_011543531.1:p.Thr237Ser
XM_011545230.1:c.616A>T	XP_011543532.1:p.Thr206Ser
XM_011545231.1:c.391A>T	XP_011543533.1:p.Thr131Ser
XM_011545232.1:c.709A>T	XP_011543534.1:p.Thr237Ser
NM_001363591.1:c.391A>T	NP_001350520.1:p.Thr131Ser
NM_001363592.1:c.709A>T	NP_001350521.1:p.Thr237Ser
NM_001363593.1:c.-467A>T	NP_001350522.1:n.-467A>T
NR_134580.1:n.1289A>T
XM_005274210.4:c.709A>T	XP_005274267.1:p.Thr237Ser
XM_005274215.4:c.391A>T	XP_005274272.1:p.Thr131Ser
XM_005274216.4:c.529A>T	XP_005274273.1:p.Thr177Ser
XM_005274219.4:c.709A>T	XP_005274276.1:p.Thr237Ser
XM_005274221.4:c.709A>T	XP_005274278.1:p.Thr237Ser
XM_011545229.3:c.709A>T	XP_011543531.1:p.Thr237Ser
XM_011545230.3:c.616A>T	XP_011543532.1:p.Thr206Ser
XM_017018230.2:c.391A>T	XP_016873719.1:p.Thr131Ser
XR_001747952.2:n.1207A>T
XR_001747953.2:n.1399A>T
XR_001747954.2:n.1399A>T
XR_001748245.1:n.1270T>A
XR_002957249.1:n.506-227T>A
NM_004183.4:c.709A>T MANE Select	NP_004174.1:p.Thr237Ser
NM_001139443.2:c.529A>T	NP_001132915.1:p.Thr177Ser
NM_001300786.2:c.529A>T	NP_001287715.1:p.Thr177Ser
NM_001300787.2:c.529A>T	NP_001287716.1:p.Thr177Ser
NM_001363591.2:c.391A>T	NP_001350520.1:p.Thr131Ser
NM_001363593.2:c.-467A>T	NP_001350522.1:n.-467A>T
NR_134580.2:n.822A>T