Canonical Allele Identifier: CA1977530292

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61956999G= , CM000673.2:g.61956999G=	GRCh38
NC_000011.9:g.61724471G= , CM000673.1:g.61724471G=	GRCh37
NC_000011.8:g.61481047G=	NCBI36
NG_009033.1:g.12116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.636+1G= MANE Select	ENSP00000367282.4:n.636+1G=
ENST00000378043.8:c.636+1G=	ENSP00000367282.4:n.636+1G=
ENST00000449131.6:c.456+1G=	ENSP00000399709.2:n.456+1G=
ENST00000524877.5:n.1068+1G=
ENST00000524926.5:c.636+1G=	ENSP00000432681.1:n.636+1G=
ENST00000526988.1:c.318+1G=	ENSP00000433195.1:n.318+1G=
ENST00000529265.5:n.559+1G=
ENST00000534553.5:c.163+1048G=	ENSP00000431189.1:n.163+1048G=
NM_001139443.1:c.456+1G=	NP_001132915.1:n.456+1G=
NM_001300786.1:c.456+1G=	NP_001287715.1:n.456+1G=
NM_001300787.1:c.456+1G=	NP_001287716.1:n.456+1G=
NM_004183.3:c.636+1G=	NP_004174.1:n.636+1G=
XM_005274210.2:c.636+1G=	XP_005274267.1:n.636+1G=
XM_005274215.2:c.318+1G=	XP_005274272.1:n.318+1G=
XM_005274216.2:c.456+1G=	XP_005274273.1:n.456+1G=
XM_005274218.3:c.318+1G=	XP_005274275.1:n.318+1G=
XM_005274219.2:c.636+1G=	XP_005274276.1:n.636+1G=
XM_005274221.2:c.636+1G=	XP_005274278.1:n.636+1G=
XM_011545229.1:c.636+1G=	XP_011543531.1:n.636+1G=
XM_011545230.1:c.543+1G=	XP_011543532.1:n.543+1G=
XM_011545231.1:c.318+1G=	XP_011543533.1:n.318+1G=
XM_011545232.1:c.636+1G=	XP_011543534.1:n.636+1G=
NM_001363591.1:c.318+1G=	NP_001350520.1:n.318+1G=
NM_001363592.1:c.636+1G=	NP_001350521.1:n.636+1G=
NM_001363593.1:c.-540+1G=	NP_001350522.1:n.-540+1G=
NR_134580.1:n.1216+1G=
XM_005274210.4:c.636+1G=	XP_005274267.1:n.636+1G=
XM_005274215.4:c.318+1G=	XP_005274272.1:n.318+1G=
XM_005274216.4:c.456+1G=	XP_005274273.1:n.456+1G=
XM_005274219.4:c.636+1G=	XP_005274276.1:n.636+1G=
XM_005274221.4:c.636+1G=	XP_005274278.1:n.636+1G=
XM_011545229.3:c.636+1G=	XP_011543531.1:n.636+1G=
XM_011545230.3:c.543+1G=	XP_011543532.1:n.543+1G=
XM_017018230.2:c.318+1G=	XP_016873719.1:n.318+1G=
XR_001747952.2:n.1134+1G=
XR_001747953.2:n.1326+1G=
XR_001747954.2:n.1326+1G=
XR_002957249.1:n.739C=
NM_004183.4:c.636+1G= MANE Select	NP_004174.1:n.636+1G=
NM_001139443.2:c.456+1G=	NP_001132915.1:n.456+1G=
NM_001300786.2:c.456+1G=	NP_001287715.1:n.456+1G=
NM_001300787.2:c.456+1G=	NP_001287716.1:n.456+1G=
NM_001363591.2:c.318+1G=	NP_001350520.1:n.318+1G=
NM_001363593.2:c.-540+1G=	NP_001350522.1:n.-540+1G=
NR_134580.2:n.749+1G=