Canonical Allele Identifier: CA2792335777

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61959330_61959412del , CM000673.2:g.61959330_61959412del	GRCh38
NC_000011.9:g.61726802_61726884del , CM000673.1:g.61726802_61726884del	GRCh37
NC_000011.8:g.61483378_61483460del	NCBI36
NG_009033.1:g.14447_14529del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378043.9:c.868-168_868-86del MANE Select	ENSP00000367282.4:n.868-168_868-86del
ENST00000378043.8:c.868-168_868-86del	ENSP00000367282.4:n.868-168_868-86del
ENST00000449131.6:c.688-168_688-86del	ENSP00000399709.2:n.688-168_688-86del
ENST00000524877.5:n.2331_2413del
ENST00000524926.5:c.1071-168_1071-86del	ENSP00000432681.1:n.1071-168_1071-86del
ENST00000526988.1:c.753-168_753-86del	ENSP00000433195.1:n.753-168_753-86del
ENST00000534553.5:c.164-2925_164-2843del	ENSP00000431189.1:n.164-2925_164-2843del
NM_001139443.1:c.688-168_688-86del	NP_001132915.1:n.688-168_688-86del
NM_001300786.1:c.688-562_688-480del	NP_001287715.1:n.688-562_688-480del
NM_001300787.1:c.688-168_688-86del	NP_001287716.1:n.688-168_688-86del
NM_004183.3:c.868-168_868-86del	NP_004174.1:n.868-168_868-86del
XM_005274210.2:c.868-168_868-86del	XP_005274267.1:n.868-168_868-86del
XM_005274215.2:c.550-168_550-86del	XP_005274272.1:n.550-168_550-86del
XM_005274216.2:c.891-168_891-86del	XP_005274273.1:n.891-168_891-86del
XM_005274218.3:c.753-168_753-86del	XP_005274275.1:n.753-168_753-86del
XM_005274219.2:c.867+1032_867+1114del	XP_005274276.1:n.867+1032_867+1114del
XM_005274221.2:c.714+1866_714+1948del	XP_005274278.1:n.714+1866_714+1948del
XM_011545229.1:c.868-168_868-86del	XP_011543531.1:n.868-168_868-86del
XM_011545230.1:c.775-168_775-86del	XP_011543532.1:n.775-168_775-86del
XM_011545231.1:c.550-168_550-86del	XP_011543533.1:n.550-168_550-86del
XM_011545232.1:c.1071-168_1071-86del	XP_011543534.1:n.1071-168_1071-86del
XM_011545233.1:c.24+125_25-86del	XP_011543535.1:n.24+125_25-86del
NM_001363591.1:c.550-168_550-86del	NP_001350520.1:n.550-168_550-86del
NM_001363592.1:c.1071-168_1071-86del	NP_001350521.1:n.1071-168_1071-86del
NM_001363593.1:c.-105-168_-105-86del	NP_001350522.1:n.-105-168_-105-86del
NR_134580.1:n.1651-168_1651-86del
XM_005274210.4:c.868-168_868-86del	XP_005274267.1:n.868-168_868-86del
XM_005274215.4:c.550-168_550-86del	XP_005274272.1:n.550-168_550-86del
XM_005274216.4:c.891-168_891-86del	XP_005274273.1:n.891-168_891-86del
XM_005274219.4:c.867+1032_867+1114del	XP_005274276.1:n.867+1032_867+1114del
XM_005274221.4:c.714+1866_714+1948del	XP_005274278.1:n.714+1866_714+1948del
XM_011545229.3:c.868-168_868-86del	XP_011543531.1:n.868-168_868-86del
XM_011545230.3:c.775-168_775-86del	XP_011543532.1:n.775-168_775-86del
XM_011545233.3:c.24+125_25-86del	XP_011543535.1:n.24+125_25-86del
XM_017018230.2:c.753-168_753-86del	XP_016873719.1:n.753-168_753-86del
XR_001747952.2:n.1569-168_1569-86del
XR_001747953.2:n.1557+1032_1557+1114del
XR_001747954.2:n.1404+1866_1404+1948del
XR_001748245.1:n.196+326_196+408del
XR_002957249.1:n.196+326_196+408del
NM_004183.4:c.868-168_868-86del MANE Select	NP_004174.1:n.868-168_868-86del
NM_001139443.2:c.688-168_688-86del	NP_001132915.1:n.688-168_688-86del
NM_001300786.2:c.688-562_688-480del	NP_001287715.1:n.688-562_688-480del
NM_001300787.2:c.688-168_688-86del	NP_001287716.1:n.688-168_688-86del
NM_001363591.2:c.550-168_550-86del	NP_001350520.1:n.550-168_550-86del
NM_001363593.2:c.-105-168_-105-86del	NP_001350522.1:n.-105-168_-105-86del
NR_134580.2:n.1184-168_1184-86del