Canonical Allele Identifier: CA2792344334

Gene: BEST1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61950483_61950484del , CM000673.2:g.61950483_61950484del	GRCh38
NC_000011.9:g.61717955_61717956del , CM000673.1:g.61717955_61717956del	GRCh37
NC_000011.8:g.61474531_61474532del	NCBI36
NG_009033.1:g.5600_5601del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378043.9:c.-37+56_-37+57del MANE Select	ENSP00000367282.4:n.-37+56_-37+57del
ENST00000378043.8:c.-37+56_-37+57del	ENSP00000367282.4:n.-37+56_-37+57del
ENST00000449131.6:c.-29+56_-29+57del	ENSP00000399709.2:n.-29+56_-29+57del
ENST00000524877.5:n.68+56_68+57del
ENST00000524926.5:c.-37+56_-37+57del	ENSP00000432681.1:n.-37+56_-37+57del
ENST00000529265.5:n.75+56_75+57del
ENST00000533521.5:n.72+56_72+57del
ENST00000534553.5:c.-212+56_-212+57del	ENSP00000431189.1:n.-212+56_-212+57del
NM_001139443.1:c.-29+56_-29+57del	NP_001132915.1:n.-29+56_-29+57del
NM_001300786.1:c.-29+56_-29+57del	NP_001287715.1:n.-29+56_-29+57del
NM_001300787.1:c.-29+56_-29+57del	NP_001287716.1:n.-29+56_-29+57del
NM_004183.3:c.-37+56_-37+57del	NP_004174.1:n.-37+56_-37+57del
XM_005274210.2:c.-37+56_-37+57del	XP_005274267.1:n.-37+56_-37+57del
XM_005274216.2:c.-29+56_-29+57del	XP_005274273.1:n.-29+56_-29+57del
XM_005274218.3:c.-212+56_-212+57del	XP_005274275.1:n.-212+56_-212+57del
XM_005274219.2:c.-37+56_-37+57del	XP_005274276.1:n.-37+56_-37+57del
XM_005274221.2:c.-37+56_-37+57del	XP_005274278.1:n.-37+56_-37+57del
XM_011545229.1:c.-36-1288_-36-1287del	XP_011543531.1:n.-36-1288_-36-1287del
XM_011545230.1:c.59+3668_59+3669del	XP_011543532.1:n.59+3668_59+3669del
XM_011545231.1:c.-212+56_-212+57del	XP_011543533.1:n.-212+56_-212+57del
XM_011545232.1:c.-37+56_-37+57del	XP_011543534.1:n.-37+56_-37+57del
NM_001363592.1:c.-37+56_-37+57del	NP_001350521.1:n.-37+56_-37+57del
NR_134580.1:n.544+56_544+57del
XM_005274210.4:c.-37+56_-37+57del	XP_005274267.1:n.-37+56_-37+57del
XM_005274216.4:c.-29+56_-29+57del	XP_005274273.1:n.-29+56_-29+57del
XM_005274219.4:c.-37+56_-37+57del	XP_005274276.1:n.-37+56_-37+57del
XM_005274221.4:c.-37+56_-37+57del	XP_005274278.1:n.-37+56_-37+57del
XM_011545229.3:c.-36-1288_-36-1287del	XP_011543531.1:n.-36-1288_-36-1287del
XM_011545230.3:c.59+3668_59+3669del	XP_011543532.1:n.59+3668_59+3669del
XR_001747952.2:n.650+56_650+57del
XR_001747953.2:n.654+56_654+57del
XR_001747954.2:n.654+56_654+57del
NM_004183.4:c.-37+56_-37+57del MANE Select	NP_004174.1:n.-37+56_-37+57del
NM_001139443.2:c.-29+56_-29+57del	NP_001132915.1:n.-29+56_-29+57del
NM_001300786.2:c.-29+56_-29+57del	NP_001287715.1:n.-29+56_-29+57del
NM_001300787.2:c.-29+56_-29+57del	NP_001287716.1:n.-29+56_-29+57del
NR_134580.2:n.77+56_77+57del