Canonical Allele Identifier: CA6040696

Gene: BEST1

Linked Data

• ClinVar Variation Id: 1291867
• ClinVar RCV Id: RCV001716944
• dbSNP Id: rs775520760
• ExAC: 11:61722565 A / C
• gnomAD v2: 11-61722565-A-C
• gnomAD v3: 11-61955093-A-C
• gnomAD v4: 11-61955093-A-C
• COSMIC: COSN20466426
• MyVariant Identifiers: chr11:g.61722565A>C (hg19) ; chr11:g.61955093A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61955093A>C , CM000673.2:g.61955093A>C	GRCh38
NC_000011.9:g.61722565A>C , CM000673.1:g.61722565A>C	GRCh37
NC_000011.8:g.61479141A>C	NCBI36
NG_009033.1:g.10210A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378043.9:c.153-14A>C MANE Select	ENSP00000367282.4:n.153-14A>C
ENST00000378043.8:c.153-14A>C	ENSP00000367282.4:n.153-14A>C
ENST00000449131.6:c.-28-14A>C	ENSP00000399709.2:n.-28-14A>C
ENST00000524877.5:n.69-14A>C
ENST00000524926.5:c.153-14A>C	ENSP00000432681.1:n.153-14A>C
ENST00000529265.5:n.76-14A>C
ENST00000533521.5:n.261-14A>C
ENST00000534553.5:c.-211-14A>C	ENSP00000431189.1:n.-211-14A>C
NM_001139443.1:c.-28-14A>C	NP_001132915.1:n.-28-14A>C
NM_001300786.1:c.-28-14A>C	NP_001287715.1:n.-28-14A>C
NM_001300787.1:c.-28-14A>C	NP_001287716.1:n.-28-14A>C
NM_004183.3:c.153-14A>C	NP_004174.1:n.153-14A>C
XM_005274210.2:c.153-14A>C	XP_005274267.1:n.153-14A>C
XM_005274216.2:c.-28-14A>C	XP_005274273.1:n.-28-14A>C
XM_005274218.3:c.-211-14A>C	XP_005274275.1:n.-211-14A>C
XM_005274219.2:c.153-14A>C	XP_005274276.1:n.153-14A>C
XM_005274221.2:c.153-14A>C	XP_005274278.1:n.153-14A>C
XM_011545229.1:c.153-14A>C	XP_011543531.1:n.153-14A>C
XM_011545230.1:c.60-14A>C	XP_011543532.1:n.60-14A>C
XM_011545231.1:c.-211-14A>C	XP_011543533.1:n.-211-14A>C
XM_011545232.1:c.153-14A>C	XP_011543534.1:n.153-14A>C
NM_001363591.1:c.-366A>C	NP_001350520.1:n.-366A>C
NM_001363592.1:c.153-14A>C	NP_001350521.1:n.153-14A>C
NM_001363593.1:c.-1223A>C	NP_001350522.1:n.-1223A>C
NR_134580.1:n.733-14A>C
XM_005274210.4:c.153-14A>C	XP_005274267.1:n.153-14A>C
XM_005274215.4:c.-366A>C	XP_005274272.1:n.-366A>C
XM_005274216.4:c.-28-14A>C	XP_005274273.1:n.-28-14A>C
XM_005274219.4:c.153-14A>C	XP_005274276.1:n.153-14A>C
XM_005274221.4:c.153-14A>C	XP_005274278.1:n.153-14A>C
XM_011545229.3:c.153-14A>C	XP_011543531.1:n.153-14A>C
XM_011545230.3:c.60-14A>C	XP_011543532.1:n.60-14A>C
XM_017018230.2:c.-366A>C	XP_016873719.1:n.-366A>C
XR_001747952.2:n.651-14A>C
XR_001747953.2:n.843-14A>C
XR_001747954.2:n.843-14A>C
XR_002957249.1:n.2645T>G
NM_004183.4:c.153-14A>C MANE Select	NP_004174.1:n.153-14A>C
NM_001139443.2:c.-28-14A>C	NP_001132915.1:n.-28-14A>C
NM_001300786.2:c.-28-14A>C	NP_001287715.1:n.-28-14A>C
NM_001300787.2:c.-28-14A>C	NP_001287716.1:n.-28-14A>C
NR_134580.2:n.266-14A>C