Canonical Allele Identifier: CA6040751

Gene: BEST1

Linked Data

• dbSNP Id: rs778771960
• ExAC: 11:61723373 G / C
• gnomAD v2: 11-61723373-G-C
• gnomAD v4: 11-61955901-G-C
• MyVariant Identifiers: chr11:g.61723373G>C (hg19) ; chr11:g.61955901G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61955901G>C , CM000673.2:g.61955901G>C	GRCh38
NC_000011.9:g.61723373G>C , CM000673.1:g.61723373G>C	GRCh37
NC_000011.8:g.61479949G>C	NCBI36
NG_009033.1:g.11018G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378043.9:c.431G>C MANE Select	ENSP00000367282.4:p.Ser144Thr
ENST00000378043.8:c.431G>C	ENSP00000367282.4:p.Ser144Thr
ENST00000449131.6:c.251G>C	ENSP00000399709.2:p.Ser84Thr
ENST00000524877.5:n.863G>C
ENST00000524926.5:c.431G>C	ENSP00000432681.1:p.Ser144Thr
ENST00000526988.1:c.113G>C	ENSP00000433195.1:p.Ser38Thr
ENST00000529265.5:n.354G>C
ENST00000533521.5:n.1055G>C
ENST00000534553.5:c.113G>C	ENSP00000431189.1:p.Ser38Thr
NM_001139443.1:c.251G>C	NP_001132915.1:p.Ser84Thr
NM_001300786.1:c.251G>C	NP_001287715.1:p.Ser84Thr
NM_001300787.1:c.251G>C	NP_001287716.1:p.Ser84Thr
NM_004183.3:c.431G>C	NP_004174.1:p.Ser144Thr
XM_005274210.2:c.431G>C	XP_005274267.1:p.Ser144Thr
XM_005274215.2:c.113G>C	XP_005274272.1:p.Ser38Thr
XM_005274216.2:c.251G>C	XP_005274273.1:p.Ser84Thr
XM_005274218.3:c.113G>C	XP_005274275.1:p.Ser38Thr
XM_005274219.2:c.431G>C	XP_005274276.1:p.Ser144Thr
XM_005274221.2:c.431G>C	XP_005274278.1:p.Ser144Thr
XM_011545229.1:c.431G>C	XP_011543531.1:p.Ser144Thr
XM_011545230.1:c.338G>C	XP_011543532.1:p.Ser113Thr
XM_011545231.1:c.113G>C	XP_011543533.1:p.Ser38Thr
XM_011545232.1:c.431G>C	XP_011543534.1:p.Ser144Thr
NM_001363591.1:c.113G>C	NP_001350520.1:p.Ser38Thr
NM_001363592.1:c.431G>C	NP_001350521.1:p.Ser144Thr
NM_001363593.1:c.-745G>C	NP_001350522.1:n.-745G>C
NR_134580.1:n.1011G>C
XM_005274210.4:c.431G>C	XP_005274267.1:p.Ser144Thr
XM_005274215.4:c.113G>C	XP_005274272.1:p.Ser38Thr
XM_005274216.4:c.251G>C	XP_005274273.1:p.Ser84Thr
XM_005274219.4:c.431G>C	XP_005274276.1:p.Ser144Thr
XM_005274221.4:c.431G>C	XP_005274278.1:p.Ser144Thr
XM_011545229.3:c.431G>C	XP_011543531.1:p.Ser144Thr
XM_011545230.3:c.338G>C	XP_011543532.1:p.Ser113Thr
XM_017018230.2:c.113G>C	XP_016873719.1:p.Ser38Thr
XR_001747952.2:n.929G>C
XR_001747953.2:n.1121G>C
XR_001747954.2:n.1121G>C
XR_002957249.1:n.1837C>G
NM_004183.4:c.431G>C MANE Select	NP_004174.1:p.Ser144Thr
NM_001139443.2:c.251G>C	NP_001132915.1:p.Ser84Thr
NM_001300786.2:c.251G>C	NP_001287715.1:p.Ser84Thr
NM_001300787.2:c.251G>C	NP_001287716.1:p.Ser84Thr
NM_001363591.2:c.113G>C	NP_001350520.1:p.Ser38Thr
NM_001363593.2:c.-745G>C	NP_001350522.1:n.-745G>C
NR_134580.2:n.544G>C