Canonical Allele Identifier: CA227837

Gene: BEST1

Linked Data

• ClinVar Variation Id: 99767
• ClinVar RCV Id: RCV000086185
• dbSNP Id: rs281865257
• MyVariant Identifiers: chr11:g.61726995T>C (hg19) ; chr11:g.61959523T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959523T>C , CM000673.2:g.61959523T>C	GRCh38
NC_000011.9:g.61726995T>C , CM000673.1:g.61726995T>C	GRCh37
NC_000011.8:g.61483571T>C	NCBI36
NG_009033.1:g.14640T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.893T>C MANE Select	ENSP00000367282.4:p.Phe298Ser
ENST00000378043.8:c.893T>C	ENSP00000367282.4:p.Phe298Ser
ENST00000449131.6:c.713T>C	ENSP00000399709.2:p.Phe238Ser
ENST00000524877.5:n.2524T>C
ENST00000524926.5:c.1096T>C	ENSP00000432681.1:p.Leu366=
ENST00000526988.1:c.778T>C	ENSP00000433195.1:p.Leu260=
ENST00000534553.5:c.164-2732T>C	ENSP00000431189.1:n.164-2732T>C
NM_001139443.1:c.713T>C	NP_001132915.1:p.Phe238Ser
NM_001300786.1:c.688-369T>C	NP_001287715.1:n.688-369T>C
NM_001300787.1:c.713T>C	NP_001287716.1:p.Phe238Ser
NM_004183.3:c.893T>C	NP_004174.1:p.Phe298Ser
XM_005274210.2:c.893T>C	XP_005274267.1:p.Phe298Ser
XM_005274215.2:c.575T>C	XP_005274272.1:p.Phe192Ser
XM_005274216.2:c.916T>C	XP_005274273.1:p.Leu306=
XM_005274218.3:c.778T>C	XP_005274275.1:p.Leu260=
XM_005274219.2:c.867+1225T>C	XP_005274276.1:n.867+1225T>C
XM_005274221.2:c.714+2059T>C	XP_005274278.1:n.714+2059T>C
XM_011545229.1:c.893T>C	XP_011543531.1:p.Phe298Ser
XM_011545230.1:c.800T>C	XP_011543532.1:p.Phe267Ser
XM_011545231.1:c.575T>C	XP_011543533.1:p.Phe192Ser
XM_011545232.1:c.1096T>C	XP_011543534.1:p.Leu366=
XM_011545233.1:c.50T>C	XP_011543535.1:p.Phe17Ser
NM_001363591.1:c.575T>C	NP_001350520.1:p.Phe192Ser
NM_001363592.1:c.1096T>C	NP_001350521.1:p.Leu366=
NM_001363593.1:c.-80T>C	NP_001350522.1:n.-80T>C
NR_134580.1:n.1676T>C
XM_005274210.4:c.893T>C	XP_005274267.1:p.Phe298Ser
XM_005274215.4:c.575T>C	XP_005274272.1:p.Phe192Ser
XM_005274216.4:c.916T>C	XP_005274273.1:p.Leu306=
XM_005274219.4:c.867+1225T>C	XP_005274276.1:n.867+1225T>C
XM_005274221.4:c.714+2059T>C	XP_005274278.1:n.714+2059T>C
XM_011545229.3:c.893T>C	XP_011543531.1:p.Phe298Ser
XM_011545230.3:c.800T>C	XP_011543532.1:p.Phe267Ser
XM_011545233.3:c.50T>C	XP_011543535.1:p.Phe17Ser
XM_017018230.2:c.778T>C	XP_016873719.1:p.Leu260=
XR_001747952.2:n.1594T>C
XR_001747953.2:n.1557+1225T>C
XR_001747954.2:n.1404+2059T>C
XR_001748245.1:n.196+209A>G
XR_002957249.1:n.196+209A>G
NM_004183.4:c.893T>C MANE Select	NP_004174.1:p.Phe298Ser
NM_001139443.2:c.713T>C	NP_001132915.1:p.Phe238Ser
NM_001300786.2:c.688-369T>C	NP_001287715.1:n.688-369T>C
NM_001300787.2:c.713T>C	NP_001287716.1:p.Phe238Ser
NM_001363591.2:c.575T>C	NP_001350520.1:p.Phe192Ser
NM_001363593.2:c.-80T>C	NP_001350522.1:n.-80T>C
NR_134580.2:n.1209T>C