Canonical Allele Identifier: CA227800

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61957415G>T , CM000673.2:g.61957415G>T	GRCh38
NC_000011.9:g.61724887G>T , CM000673.1:g.61724887G>T	GRCh37
NC_000011.8:g.61481463G>T	NCBI36
NG_009033.1:g.12532G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004183.4:c.665G>T MANE Select	NP_004174.1:p.Gly222Val
ENST00000378043.9:c.665G>T MANE Select	ENSP00000367282.4:p.Gly222Val
NM_001139443.1:c.485G>T	NP_001132915.1:p.Gly162Val
NM_001139443.2:c.485G>T	NP_001132915.1:p.Gly162Val
NM_001300786.1:c.485G>T	NP_001287715.1:p.Gly162Val
NM_001300786.2:c.485G>T	NP_001287715.1:p.Gly162Val
NM_001300787.1:c.485G>T	NP_001287716.1:p.Gly162Val
NM_001300787.2:c.485G>T	NP_001287716.1:p.Gly162Val
NM_001363591.1:c.347G>T	NP_001350520.1:p.Gly116Val
NM_001363591.2:c.347G>T	NP_001350520.1:p.Gly116Val
NM_001363592.1:c.665G>T	NP_001350521.1:p.Gly222Val
NM_001363593.1:c.-511G>T	NP_001350522.1:n.-511G>T
NM_001363593.2:c.-511G>T	NP_001350522.1:n.-511G>T
NM_004183.3:c.665G>T	NP_004174.1:p.Gly222Val
NR_134580.1:n.1245G>T
NR_134580.2:n.778G>T
ENST00000378043.8:c.665G>T	ENSP00000367282.4:p.Gly222Val
ENST00000449131.6:c.485G>T	ENSP00000399709.2:p.Gly162Val
ENST00000524877.5:n.1097G>T
ENST00000524926.5:c.665G>T	ENSP00000432681.1:p.Gly222Val
ENST00000526988.1:c.347G>T	ENSP00000433195.1:p.Gly116Val
ENST00000529265.5:n.588G>T
ENST00000534553.5:c.163+1464G>T	ENSP00000431189.1:n.163+1464G>T
XM_005274210.2:c.665G>T	XP_005274267.1:p.Gly222Val
XM_005274210.4:c.665G>T	XP_005274267.1:p.Gly222Val
XM_005274215.2:c.347G>T	XP_005274272.1:p.Gly116Val
XM_005274215.4:c.347G>T	XP_005274272.1:p.Gly116Val
XM_005274216.2:c.485G>T	XP_005274273.1:p.Gly162Val
XM_005274216.4:c.485G>T	XP_005274273.1:p.Gly162Val
XM_005274218.3:c.347G>T	XP_005274275.1:p.Gly116Val
XM_005274219.2:c.665G>T	XP_005274276.1:p.Gly222Val
XM_005274219.4:c.665G>T	XP_005274276.1:p.Gly222Val
XM_005274221.2:c.665G>T	XP_005274278.1:p.Gly222Val
XM_005274221.4:c.665G>T	XP_005274278.1:p.Gly222Val
XM_011545229.1:c.665G>T	XP_011543531.1:p.Gly222Val
XM_011545229.3:c.665G>T	XP_011543531.1:p.Gly222Val
XM_011545230.1:c.572G>T	XP_011543532.1:p.Gly191Val
XM_011545230.3:c.572G>T	XP_011543532.1:p.Gly191Val
XM_011545231.1:c.347G>T	XP_011543533.1:p.Gly116Val
XM_011545232.1:c.665G>T	XP_011543534.1:p.Gly222Val
XM_017018230.2:c.347G>T	XP_016873719.1:p.Gly116Val
XR_001747952.2:n.1163G>T
XR_001747953.2:n.1355G>T
XR_001747954.2:n.1355G>T
XR_001748245.1:n.1314C>A
XR_002957249.1:n.506-183C>A