Canonical Allele Identifier: CA1977534639

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959892G= , CM000673.2:g.61959892G= GRCh38
NC_000011.9:g.61727364G= , CM000673.1:g.61727364G= GRCh37
NC_000011.8:g.61483940G= NCBI36
NG_009033.1:g.15009G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.949G= (BEST1) MANE Select ENSP00000367282.4:p.Val317=
ENST00000378043.8:c.949G= (BEST1) ENSP00000367282.4:p.Val317=
ENST00000449131.6:c.769G= (BEST1) ENSP00000399709.2:p.Val257=
ENST00000524877.5:n.2580G= (BEST1)
ENST00000524926.5:c.1152G= (BEST1) ENSP00000432681.1:p.Arg384=
ENST00000526988.1:c.834G= (BEST1) ENSP00000433195.1:p.Arg278=
ENST00000529191.5:c.150C= (FTH1) ENSP00000431659.1:p.His50=
ENST00000529631.5:c.127C= (FTH1) ENSP00000431575.1:p.Pro43=
ENST00000530019.5:c.274C= (FTH1) ENSP00000433470.1:p.Pro92=
ENST00000534553.5:c.164-2363G= (BEST1) ENSP00000431189.1:n.164-2363G=
NM_001139443.1:c.769G= (BEST1) NP_001132915.1:p.Val257=
NM_001300786.1:c.688G= (BEST1) NP_001287715.1:p.Val230=
NM_001300787.1:c.769G= (BEST1) NP_001287716.1:p.Val257=
NM_004183.3:c.949G= (BEST1) NP_004174.1:p.Val317=
XM_005274210.2:c.949G= (BEST1) XP_005274267.1:p.Val317=
XM_005274215.2:c.631G= (BEST1) XP_005274272.1:p.Val211=
XM_005274216.2:c.972G= (BEST1) XP_005274273.1:p.Arg324=
XM_005274218.3:c.834G= (BEST1) XP_005274275.1:p.Arg278=
XM_005274219.2:c.867+1594G= (BEST1) XP_005274276.1:n.867+1594G=
XM_005274221.2:c.715-2363G= (BEST1) XP_005274278.1:n.715-2363G=
XM_011545229.1:c.949G= (BEST1) XP_011543531.1:p.Val317=
XM_011545230.1:c.856G= (BEST1) XP_011543532.1:p.Val286=
XM_011545231.1:c.631G= (BEST1) XP_011543533.1:p.Val211=
XM_011545232.1:c.1152G= (BEST1) XP_011543534.1:p.Arg384=
XM_011545233.1:c.106G= (BEST1) XP_011543535.1:p.Val36=
NM_001363591.1:c.631G= (BEST1) NP_001350520.1:p.Val211=
NM_001363592.1:c.1152G= (BEST1) NP_001350521.1:p.Arg384=
NM_001363593.1:c.-24G= (BEST1) NP_001350522.1:n.-24G=
NR_134580.1:n.1732G= (BEST1)
XM_005274210.4:c.949G= (BEST1) XP_005274267.1:p.Val317=
XM_005274215.4:c.631G= (BEST1) XP_005274272.1:p.Val211=
XM_005274216.4:c.972G= (BEST1) XP_005274273.1:p.Arg324=
XM_005274219.4:c.867+1594G= (BEST1) XP_005274276.1:n.867+1594G=
XM_005274221.4:c.715-2363G= (BEST1) XP_005274278.1:n.715-2363G=
XM_011545229.3:c.949G= (BEST1) XP_011543531.1:p.Val317=
XM_011545230.3:c.856G= (BEST1) XP_011543532.1:p.Val286=
XM_011545233.3:c.106G= (BEST1) XP_011543535.1:p.Val36=
XM_017018230.2:c.834G= (BEST1) XP_016873719.1:p.Arg278=
XR_001747952.2:n.1650G= (BEST1)
XR_001747953.2:n.1557+1594G= (BEST1)
XR_001747954.2:n.1405-2363G= (BEST1)
XR_001748245.1:n.36C=
XR_002957249.1:n.36C=
NM_004183.4:c.949G= (BEST1) MANE Select NP_004174.1:p.Val317=
NM_001139443.2:c.769G= (BEST1) NP_001132915.1:p.Val257=
NM_001300786.2:c.688G= (BEST1) NP_001287715.1:p.Val230=
NM_001300787.2:c.769G= (BEST1) NP_001287716.1:p.Val257=
NM_001363591.2:c.631G= (BEST1) NP_001350520.1:p.Val211=
NM_001363593.2:c.-24G= (BEST1) NP_001350522.1:n.-24G=
NR_134580.2:n.1265G= (BEST1)