Canonical Allele Identifier: CA380843764

Gene: BEST1

Linked Data

• MyVariant Identifiers: chr11:g.61726991C>A (hg19) ; chr11:g.61959519C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959519C>A , CM000673.2:g.61959519C>A	GRCh38
NC_000011.9:g.61726991C>A , CM000673.1:g.61726991C>A	GRCh37
NC_000011.8:g.61483567C>A	NCBI36
NG_009033.1:g.14636C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.889C>A MANE Select	ENSP00000367282.4:p.Pro297Thr
ENST00000378043.8:c.889C>A	ENSP00000367282.4:p.Pro297Thr
ENST00000449131.6:c.709C>A	ENSP00000399709.2:p.Pro237Thr
ENST00000524877.5:n.2520C>A
ENST00000524926.5:c.1092C>A	ENSP00000432681.1:p.Thr364=
ENST00000526988.1:c.774C>A	ENSP00000433195.1:p.Thr258=
ENST00000534553.5:c.164-2736C>A	ENSP00000431189.1:n.164-2736C>A
NM_001139443.1:c.709C>A	NP_001132915.1:p.Pro237Thr
NM_001300786.1:c.688-373C>A	NP_001287715.1:n.688-373C>A
NM_001300787.1:c.709C>A	NP_001287716.1:p.Pro237Thr
NM_004183.3:c.889C>A	NP_004174.1:p.Pro297Thr
XM_005274210.2:c.889C>A	XP_005274267.1:p.Pro297Thr
XM_005274215.2:c.571C>A	XP_005274272.1:p.Pro191Thr
XM_005274216.2:c.912C>A	XP_005274273.1:p.Thr304=
XM_005274218.3:c.774C>A	XP_005274275.1:p.Thr258=
XM_005274219.2:c.867+1221C>A	XP_005274276.1:n.867+1221C>A
XM_005274221.2:c.714+2055C>A	XP_005274278.1:n.714+2055C>A
XM_011545229.1:c.889C>A	XP_011543531.1:p.Pro297Thr
XM_011545230.1:c.796C>A	XP_011543532.1:p.Pro266Thr
XM_011545231.1:c.571C>A	XP_011543533.1:p.Pro191Thr
XM_011545232.1:c.1092C>A	XP_011543534.1:p.Thr364=
XM_011545233.1:c.46C>A	XP_011543535.1:p.Pro16Thr
NM_001363591.1:c.571C>A	NP_001350520.1:p.Pro191Thr
NM_001363592.1:c.1092C>A	NP_001350521.1:p.Thr364=
NM_001363593.1:c.-84C>A	NP_001350522.1:n.-84C>A
NR_134580.1:n.1672C>A
XM_005274210.4:c.889C>A	XP_005274267.1:p.Pro297Thr
XM_005274215.4:c.571C>A	XP_005274272.1:p.Pro191Thr
XM_005274216.4:c.912C>A	XP_005274273.1:p.Thr304=
XM_005274219.4:c.867+1221C>A	XP_005274276.1:n.867+1221C>A
XM_005274221.4:c.714+2055C>A	XP_005274278.1:n.714+2055C>A
XM_011545229.3:c.889C>A	XP_011543531.1:p.Pro297Thr
XM_011545230.3:c.796C>A	XP_011543532.1:p.Pro266Thr
XM_011545233.3:c.46C>A	XP_011543535.1:p.Pro16Thr
XM_017018230.2:c.774C>A	XP_016873719.1:p.Thr258=
XR_001747952.2:n.1590C>A
XR_001747953.2:n.1557+1221C>A
XR_001747954.2:n.1404+2055C>A
XR_001748245.1:n.196+213G>T
XR_002957249.1:n.196+213G>T
NM_004183.4:c.889C>A MANE Select	NP_004174.1:p.Pro297Thr
NM_001139443.2:c.709C>A	NP_001132915.1:p.Pro237Thr
NM_001300786.2:c.688-373C>A	NP_001287715.1:n.688-373C>A
NM_001300787.2:c.709C>A	NP_001287716.1:p.Pro237Thr
NM_001363591.2:c.571C>A	NP_001350520.1:p.Pro191Thr
NM_001363593.2:c.-84C>A	NP_001350522.1:n.-84C>A
NR_134580.2:n.1205C>A