Canonical Allele Identifier: CA380843604

Gene: BEST1

Linked Data

• MyVariant Identifiers: chr11:g.61726974C>A (hg19) ; chr11:g.61959502C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959502C>A , CM000673.2:g.61959502C>A	GRCh38
NC_000011.9:g.61726974C>A , CM000673.1:g.61726974C>A	GRCh37
NC_000011.8:g.61483550C>A	NCBI36
NG_009033.1:g.14619C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.872C>A MANE Select	ENSP00000367282.4:p.Ala291Glu
ENST00000378043.8:c.872C>A	ENSP00000367282.4:p.Ala291Glu
ENST00000449131.6:c.692C>A	ENSP00000399709.2:p.Ala231Glu
ENST00000524877.5:n.2503C>A
ENST00000524926.5:c.1075C>A	ENSP00000432681.1:p.Gln359Lys
ENST00000526988.1:c.757C>A	ENSP00000433195.1:p.Gln253Lys
ENST00000534553.5:c.164-2753C>A	ENSP00000431189.1:n.164-2753C>A
NM_001139443.1:c.692C>A	NP_001132915.1:p.Ala231Glu
NM_001300786.1:c.688-390C>A	NP_001287715.1:n.688-390C>A
NM_001300787.1:c.692C>A	NP_001287716.1:p.Ala231Glu
NM_004183.3:c.872C>A	NP_004174.1:p.Ala291Glu
XM_005274210.2:c.872C>A	XP_005274267.1:p.Ala291Glu
XM_005274215.2:c.554C>A	XP_005274272.1:p.Ala185Glu
XM_005274216.2:c.895C>A	XP_005274273.1:p.Gln299Lys
XM_005274218.3:c.757C>A	XP_005274275.1:p.Gln253Lys
XM_005274219.2:c.867+1204C>A	XP_005274276.1:n.867+1204C>A
XM_005274221.2:c.714+2038C>A	XP_005274278.1:n.714+2038C>A
XM_011545229.1:c.872C>A	XP_011543531.1:p.Ala291Glu
XM_011545230.1:c.779C>A	XP_011543532.1:p.Ala260Glu
XM_011545231.1:c.554C>A	XP_011543533.1:p.Ala185Glu
XM_011545232.1:c.1075C>A	XP_011543534.1:p.Gln359Lys
XM_011545233.1:c.29C>A	XP_011543535.1:p.Ala10Glu
NM_001363591.1:c.554C>A	NP_001350520.1:p.Ala185Glu
NM_001363592.1:c.1075C>A	NP_001350521.1:p.Gln359Lys
NM_001363593.1:c.-101C>A	NP_001350522.1:n.-101C>A
NR_134580.1:n.1655C>A
XM_005274210.4:c.872C>A	XP_005274267.1:p.Ala291Glu
XM_005274215.4:c.554C>A	XP_005274272.1:p.Ala185Glu
XM_005274216.4:c.895C>A	XP_005274273.1:p.Gln299Lys
XM_005274219.4:c.867+1204C>A	XP_005274276.1:n.867+1204C>A
XM_005274221.4:c.714+2038C>A	XP_005274278.1:n.714+2038C>A
XM_011545229.3:c.872C>A	XP_011543531.1:p.Ala291Glu
XM_011545230.3:c.779C>A	XP_011543532.1:p.Ala260Glu
XM_011545233.3:c.29C>A	XP_011543535.1:p.Ala10Glu
XM_017018230.2:c.757C>A	XP_016873719.1:p.Gln253Lys
XR_001747952.2:n.1573C>A
XR_001747953.2:n.1557+1204C>A
XR_001747954.2:n.1404+2038C>A
XR_001748245.1:n.196+230G>T
XR_002957249.1:n.196+230G>T
NM_004183.4:c.872C>A MANE Select	NP_004174.1:p.Ala291Glu
NM_001139443.2:c.692C>A	NP_001132915.1:p.Ala231Glu
NM_001300786.2:c.688-390C>A	NP_001287715.1:n.688-390C>A
NM_001300787.2:c.692C>A	NP_001287716.1:p.Ala231Glu
NM_001363591.2:c.554C>A	NP_001350520.1:p.Ala185Glu
NM_001363593.2:c.-101C>A	NP_001350522.1:n.-101C>A
NR_134580.2:n.1188C>A