Canonical Allele Identifier: CA678994389

Gene: BEST1

Linked Data

• dbSNP Id: rs1169486789
• gnomAD v3: 11-61959677-T-C
• gnomAD v4: 11-61959677-T-C
• MyVariant Identifiers: chr11:g.61727149T>C (hg19) ; chr11:g.61959677T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959677T>C , CM000673.2:g.61959677T>C	GRCh38
NC_000011.9:g.61727149T>C , CM000673.1:g.61727149T>C	GRCh37
NC_000011.8:g.61483725T>C	NCBI36
NG_009033.1:g.14794T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.948+99T>C MANE Select	ENSP00000367282.4:n.948+99T>C
ENST00000378043.8:c.948+99T>C	ENSP00000367282.4:n.948+99T>C
ENST00000449131.6:c.768+99T>C	ENSP00000399709.2:n.768+99T>C
ENST00000524877.5:n.2579+99T>C
ENST00000524926.5:c.1151+99T>C	ENSP00000432681.1:n.1151+99T>C
ENST00000526988.1:c.833+99T>C	ENSP00000433195.1:n.833+99T>C
ENST00000534553.5:c.164-2578T>C	ENSP00000431189.1:n.164-2578T>C
NM_001139443.1:c.768+99T>C	NP_001132915.1:n.768+99T>C
NM_001300786.1:c.688-215T>C	NP_001287715.1:n.688-215T>C
NM_001300787.1:c.768+99T>C	NP_001287716.1:n.768+99T>C
NM_004183.3:c.948+99T>C	NP_004174.1:n.948+99T>C
XM_005274210.2:c.948+99T>C	XP_005274267.1:n.948+99T>C
XM_005274215.2:c.630+99T>C	XP_005274272.1:n.630+99T>C
XM_005274216.2:c.971+99T>C	XP_005274273.1:n.971+99T>C
XM_005274218.3:c.833+99T>C	XP_005274275.1:n.833+99T>C
XM_005274219.2:c.867+1379T>C	XP_005274276.1:n.867+1379T>C
XM_005274221.2:c.714+2213T>C	XP_005274278.1:n.714+2213T>C
XM_011545229.1:c.948+99T>C	XP_011543531.1:n.948+99T>C
XM_011545230.1:c.855+99T>C	XP_011543532.1:n.855+99T>C
XM_011545231.1:c.630+99T>C	XP_011543533.1:n.630+99T>C
XM_011545232.1:c.1151+99T>C	XP_011543534.1:n.1151+99T>C
XM_011545233.1:c.105+99T>C	XP_011543535.1:n.105+99T>C
NM_001363591.1:c.630+99T>C	NP_001350520.1:n.630+99T>C
NM_001363592.1:c.1151+99T>C	NP_001350521.1:n.1151+99T>C
NM_001363593.1:c.-25+99T>C	NP_001350522.1:n.-25+99T>C
NR_134580.1:n.1731+99T>C
XM_005274210.4:c.948+99T>C	XP_005274267.1:n.948+99T>C
XM_005274215.4:c.630+99T>C	XP_005274272.1:n.630+99T>C
XM_005274216.4:c.971+99T>C	XP_005274273.1:n.971+99T>C
XM_005274219.4:c.867+1379T>C	XP_005274276.1:n.867+1379T>C
XM_005274221.4:c.714+2213T>C	XP_005274278.1:n.714+2213T>C
XM_011545229.3:c.948+99T>C	XP_011543531.1:n.948+99T>C
XM_011545230.3:c.855+99T>C	XP_011543532.1:n.855+99T>C
XM_011545233.3:c.105+99T>C	XP_011543535.1:n.105+99T>C
XM_017018230.2:c.833+99T>C	XP_016873719.1:n.833+99T>C
XR_001747952.2:n.1649+99T>C
XR_001747953.2:n.1557+1379T>C
XR_001747954.2:n.1404+2213T>C
XR_001748245.1:n.196+55A>G
XR_002957249.1:n.196+55A>G
NM_004183.4:c.948+99T>C MANE Select	NP_004174.1:n.948+99T>C
NM_001139443.2:c.768+99T>C	NP_001132915.1:n.768+99T>C
NM_001300786.2:c.688-215T>C	NP_001287715.1:n.688-215T>C
NM_001300787.2:c.768+99T>C	NP_001287716.1:n.768+99T>C
NM_001363591.2:c.630+99T>C	NP_001350520.1:n.630+99T>C
NM_001363593.2:c.-25+99T>C	NP_001350522.1:n.-25+99T>C
NR_134580.2:n.1264+99T>C