Canonical Allele Identifier: CA380843713

Gene: BEST1

Linked Data

• ClinVar Variation Id: 950125
• ClinVar RCV Id: RCV001221767
• dbSNP Id: rs777320382
• MyVariant Identifiers: chr11:g.61726985A>C (hg19) ; chr11:g.61959513A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959513A>C , CM000673.2:g.61959513A>C	GRCh38
NC_000011.9:g.61726985A>C , CM000673.1:g.61726985A>C	GRCh37
NC_000011.8:g.61483561A>C	NCBI36
NG_009033.1:g.14630A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.883A>C MANE Select	ENSP00000367282.4:p.Ile295Leu
ENST00000378043.8:c.883A>C	ENSP00000367282.4:p.Ile295Leu
ENST00000449131.6:c.703A>C	ENSP00000399709.2:p.Ile235Leu
ENST00000524877.5:n.2514A>C
ENST00000524926.5:c.1086A>C	ENSP00000432681.1:p.Ser362=
ENST00000526988.1:c.768A>C	ENSP00000433195.1:p.Ser256=
ENST00000534553.5:c.164-2742A>C	ENSP00000431189.1:n.164-2742A>C
NM_001139443.1:c.703A>C	NP_001132915.1:p.Ile235Leu
NM_001300786.1:c.688-379A>C	NP_001287715.1:n.688-379A>C
NM_001300787.1:c.703A>C	NP_001287716.1:p.Ile235Leu
NM_004183.3:c.883A>C	NP_004174.1:p.Ile295Leu
XM_005274210.2:c.883A>C	XP_005274267.1:p.Ile295Leu
XM_005274215.2:c.565A>C	XP_005274272.1:p.Ile189Leu
XM_005274216.2:c.906A>C	XP_005274273.1:p.Ser302=
XM_005274218.3:c.768A>C	XP_005274275.1:p.Ser256=
XM_005274219.2:c.867+1215A>C	XP_005274276.1:n.867+1215A>C
XM_005274221.2:c.714+2049A>C	XP_005274278.1:n.714+2049A>C
XM_011545229.1:c.883A>C	XP_011543531.1:p.Ile295Leu
XM_011545230.1:c.790A>C	XP_011543532.1:p.Ile264Leu
XM_011545231.1:c.565A>C	XP_011543533.1:p.Ile189Leu
XM_011545232.1:c.1086A>C	XP_011543534.1:p.Ser362=
XM_011545233.1:c.40A>C	XP_011543535.1:p.Ile14Leu
NM_001363591.1:c.565A>C	NP_001350520.1:p.Ile189Leu
NM_001363592.1:c.1086A>C	NP_001350521.1:p.Ser362=
NM_001363593.1:c.-90A>C	NP_001350522.1:n.-90A>C
NR_134580.1:n.1666A>C
XM_005274210.4:c.883A>C	XP_005274267.1:p.Ile295Leu
XM_005274215.4:c.565A>C	XP_005274272.1:p.Ile189Leu
XM_005274216.4:c.906A>C	XP_005274273.1:p.Ser302=
XM_005274219.4:c.867+1215A>C	XP_005274276.1:n.867+1215A>C
XM_005274221.4:c.714+2049A>C	XP_005274278.1:n.714+2049A>C
XM_011545229.3:c.883A>C	XP_011543531.1:p.Ile295Leu
XM_011545230.3:c.790A>C	XP_011543532.1:p.Ile264Leu
XM_011545233.3:c.40A>C	XP_011543535.1:p.Ile14Leu
XM_017018230.2:c.768A>C	XP_016873719.1:p.Ser256=
XR_001747952.2:n.1584A>C
XR_001747953.2:n.1557+1215A>C
XR_001747954.2:n.1404+2049A>C
XR_001748245.1:n.196+219T>G
XR_002957249.1:n.196+219T>G
NM_004183.4:c.883A>C MANE Select	NP_004174.1:p.Ile295Leu
NM_001139443.2:c.703A>C	NP_001132915.1:p.Ile235Leu
NM_001300786.2:c.688-379A>C	NP_001287715.1:n.688-379A>C
NM_001300787.2:c.703A>C	NP_001287716.1:p.Ile235Leu
NM_001363591.2:c.565A>C	NP_001350520.1:p.Ile189Leu
NM_001363593.2:c.-90A>C	NP_001350522.1:n.-90A>C
NR_134580.2:n.1199A>C