Canonical Allele Identifier: CA380844145

Gene: BEST1

Linked Data

• MyVariant Identifiers: chr11:g.61727040G>T (hg19) ; chr11:g.61959568G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959568G>T , CM000673.2:g.61959568G>T	GRCh38
NC_000011.9:g.61727040G>T , CM000673.1:g.61727040G>T	GRCh37
NC_000011.8:g.61483616G>T	NCBI36
NG_009033.1:g.14685G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.938G>T MANE Select	ENSP00000367282.4:p.Arg313Met
ENST00000378043.8:c.938G>T	ENSP00000367282.4:p.Arg313Met
ENST00000449131.6:c.758G>T	ENSP00000399709.2:p.Arg253Met
ENST00000524877.5:n.2569G>T
ENST00000524926.5:c.1141G>T	ENSP00000432681.1:p.Gly381Ter
ENST00000526988.1:c.823G>T	ENSP00000433195.1:p.Gly275Ter
ENST00000534553.5:c.164-2687G>T	ENSP00000431189.1:n.164-2687G>T
NM_001139443.1:c.758G>T	NP_001132915.1:p.Arg253Met
NM_001300786.1:c.688-324G>T	NP_001287715.1:n.688-324G>T
NM_001300787.1:c.758G>T	NP_001287716.1:p.Arg253Met
NM_004183.3:c.938G>T	NP_004174.1:p.Arg313Met
XM_005274210.2:c.938G>T	XP_005274267.1:p.Arg313Met
XM_005274215.2:c.620G>T	XP_005274272.1:p.Arg207Met
XM_005274216.2:c.961G>T	XP_005274273.1:p.Gly321Ter
XM_005274218.3:c.823G>T	XP_005274275.1:p.Gly275Ter
XM_005274219.2:c.867+1270G>T	XP_005274276.1:n.867+1270G>T
XM_005274221.2:c.714+2104G>T	XP_005274278.1:n.714+2104G>T
XM_011545229.1:c.938G>T	XP_011543531.1:p.Arg313Met
XM_011545230.1:c.845G>T	XP_011543532.1:p.Arg282Met
XM_011545231.1:c.620G>T	XP_011543533.1:p.Arg207Met
XM_011545232.1:c.1141G>T	XP_011543534.1:p.Gly381Ter
XM_011545233.1:c.95G>T	XP_011543535.1:p.Arg32Met
NM_001363591.1:c.620G>T	NP_001350520.1:p.Arg207Met
NM_001363592.1:c.1141G>T	NP_001350521.1:p.Gly381Ter
NM_001363593.1:c.-35G>T	NP_001350522.1:n.-35G>T
NR_134580.1:n.1721G>T
XM_005274210.4:c.938G>T	XP_005274267.1:p.Arg313Met
XM_005274215.4:c.620G>T	XP_005274272.1:p.Arg207Met
XM_005274216.4:c.961G>T	XP_005274273.1:p.Gly321Ter
XM_005274219.4:c.867+1270G>T	XP_005274276.1:n.867+1270G>T
XM_005274221.4:c.714+2104G>T	XP_005274278.1:n.714+2104G>T
XM_011545229.3:c.938G>T	XP_011543531.1:p.Arg313Met
XM_011545230.3:c.845G>T	XP_011543532.1:p.Arg282Met
XM_011545233.3:c.95G>T	XP_011543535.1:p.Arg32Met
XM_017018230.2:c.823G>T	XP_016873719.1:p.Gly275Ter
XR_001747952.2:n.1639G>T
XR_001747953.2:n.1557+1270G>T
XR_001747954.2:n.1404+2104G>T
XR_001748245.1:n.196+164C>A
XR_002957249.1:n.196+164C>A
NM_004183.4:c.938G>T MANE Select	NP_004174.1:p.Arg313Met
NM_001139443.2:c.758G>T	NP_001132915.1:p.Arg253Met
NM_001300786.2:c.688-324G>T	NP_001287715.1:n.688-324G>T
NM_001300787.2:c.758G>T	NP_001287716.1:p.Arg253Met
NM_001363591.2:c.620G>T	NP_001350520.1:p.Arg207Met
NM_001363593.2:c.-35G>T	NP_001350522.1:n.-35G>T
NR_134580.2:n.1254G>T