Canonical Allele Identifier: CA599796012

Linked Data

dbSNP Id: rs1266725226

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959810_61959811del , CM000673.2:g.61959810_61959811del GRCh38
NC_000011.9:g.61727282_61727283del , CM000673.1:g.61727282_61727283del GRCh37
NC_000011.8:g.61483858_61483859del NCBI36
NG_009033.1:g.14927_14928del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.949-82_949-81del (BEST1) MANE Select ENSP00000367282.4:n.949-82_949-81del
ENST00000378043.8:c.949-82_949-81del (BEST1) ENSP00000367282.4:n.949-82_949-81del
ENST00000449131.6:c.769-82_769-81del (BEST1) ENSP00000399709.2:n.769-82_769-81del
ENST00000524877.5:n.2580-82_2580-81del (BEST1)
ENST00000524926.5:c.1152-82_1152-81del (BEST1) ENSP00000432681.1:n.1152-82_1152-81del
ENST00000526988.1:c.834-82_834-81del (BEST1) ENSP00000433195.1:n.834-82_834-81del
ENST00000529191.5:c.235_236del (FTH1) ENSP00000431659.1:p.Ser79ProfsTer11
ENST00000529631.5:c.212_213del (FTH1) ENSP00000431575.1:p.Leu71ProfsTer?
ENST00000534553.5:c.164-2445_164-2444del (BEST1) ENSP00000431189.1:n.164-2445_164-2444del
NM_001139443.1:c.769-82_769-81del (BEST1) NP_001132915.1:n.769-82_769-81del
NM_001300786.1:c.688-82_688-81del (BEST1) NP_001287715.1:n.688-82_688-81del
NM_001300787.1:c.769-82_769-81del (BEST1) NP_001287716.1:n.769-82_769-81del
NM_004183.3:c.949-82_949-81del (BEST1) NP_004174.1:n.949-82_949-81del
XM_005274210.2:c.949-82_949-81del (BEST1) XP_005274267.1:n.949-82_949-81del
XM_005274215.2:c.631-82_631-81del (BEST1) XP_005274272.1:n.631-82_631-81del
XM_005274216.2:c.972-82_972-81del (BEST1) XP_005274273.1:n.972-82_972-81del
XM_005274218.3:c.834-82_834-81del (BEST1) XP_005274275.1:n.834-82_834-81del
XM_005274219.2:c.867+1512_867+1513del (BEST1) XP_005274276.1:n.867+1512_867+1513del
XM_005274221.2:c.714+2346_714+2347del (BEST1) XP_005274278.1:n.714+2346_714+2347del
XM_011545229.1:c.949-82_949-81del (BEST1) XP_011543531.1:n.949-82_949-81del
XM_011545230.1:c.856-82_856-81del (BEST1) XP_011543532.1:n.856-82_856-81del
XM_011545231.1:c.631-82_631-81del (BEST1) XP_011543533.1:n.631-82_631-81del
XM_011545232.1:c.1152-82_1152-81del (BEST1) XP_011543534.1:n.1152-82_1152-81del
XM_011545233.1:c.106-82_106-81del (BEST1) XP_011543535.1:n.106-82_106-81del
NM_001363591.1:c.631-82_631-81del (BEST1) NP_001350520.1:n.631-82_631-81del
NM_001363592.1:c.1152-82_1152-81del (BEST1) NP_001350521.1:n.1152-82_1152-81del
NM_001363593.1:c.-24-82_-24-81del (BEST1) NP_001350522.1:n.-24-82_-24-81del
NR_134580.1:n.1732-82_1732-81del (BEST1)
XM_005274210.4:c.949-82_949-81del (BEST1) XP_005274267.1:n.949-82_949-81del
XM_005274215.4:c.631-82_631-81del (BEST1) XP_005274272.1:n.631-82_631-81del
XM_005274216.4:c.972-82_972-81del (BEST1) XP_005274273.1:n.972-82_972-81del
XM_005274219.4:c.867+1512_867+1513del (BEST1) XP_005274276.1:n.867+1512_867+1513del
XM_005274221.4:c.714+2346_714+2347del (BEST1) XP_005274278.1:n.714+2346_714+2347del
XM_011545229.3:c.949-82_949-81del (BEST1) XP_011543531.1:n.949-82_949-81del
XM_011545230.3:c.856-82_856-81del (BEST1) XP_011543532.1:n.856-82_856-81del
XM_011545233.3:c.106-82_106-81del (BEST1) XP_011543535.1:n.106-82_106-81del
XM_017018230.2:c.834-82_834-81del (BEST1) XP_016873719.1:n.834-82_834-81del
XR_001747952.2:n.1650-82_1650-81del (BEST1)
XR_001747953.2:n.1557+1512_1557+1513del (BEST1)
XR_001747954.2:n.1404+2346_1404+2347del (BEST1)
XR_001748245.1:n.121_122del
XR_002957249.1:n.121_122del
NM_004183.4:c.949-82_949-81del (BEST1) MANE Select NP_004174.1:n.949-82_949-81del
NM_001139443.2:c.769-82_769-81del (BEST1) NP_001132915.1:n.769-82_769-81del
NM_001300786.2:c.688-82_688-81del (BEST1) NP_001287715.1:n.688-82_688-81del
NM_001300787.2:c.769-82_769-81del (BEST1) NP_001287716.1:n.769-82_769-81del
NM_001363591.2:c.631-82_631-81del (BEST1) NP_001350520.1:n.631-82_631-81del
NM_001363593.2:c.-24-82_-24-81del (BEST1) NP_001350522.1:n.-24-82_-24-81del
NR_134580.2:n.1265-82_1265-81del (BEST1)