Canonical Allele Identifier: CA1977534714

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61959934C= , CM000673.2:g.61959934C= GRCh38
NC_000011.9:g.61727406C= , CM000673.1:g.61727406C= GRCh37
NC_000011.8:g.61483982C= NCBI36
NG_009033.1:g.15051C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378043.9:c.991C= (BEST1) MANE Select ENSP00000367282.4:p.Arg331=
ENST00000378043.8:c.991C= (BEST1) ENSP00000367282.4:p.Arg331=
ENST00000449131.6:c.811C= (BEST1) ENSP00000399709.2:p.Arg271=
ENST00000524877.5:n.2622C= (BEST1)
ENST00000524926.5:c.1194C= (BEST1) ENSP00000432681.1:p.Leu398=
ENST00000526988.1:c.876C= (BEST1) ENSP00000433195.1:p.Leu292=
ENST00000529191.5:c.115-7G= (FTH1) ENSP00000431659.1:n.115-7G=
ENST00000529631.5:c.115-30G= (FTH1) ENSP00000431575.1:n.115-30G=
ENST00000530019.5:c.262-30G= (FTH1) ENSP00000433470.1:n.262-30G=
ENST00000534553.5:c.164-2321C= (BEST1) ENSP00000431189.1:n.164-2321C=
NM_001139443.1:c.811C= (BEST1) NP_001132915.1:p.Arg271=
NM_001300786.1:c.730C= (BEST1) NP_001287715.1:p.Arg244=
NM_001300787.1:c.811C= (BEST1) NP_001287716.1:p.Arg271=
NM_004183.3:c.991C= (BEST1) NP_004174.1:p.Arg331=
XM_005274210.2:c.991C= (BEST1) XP_005274267.1:p.Arg331=
XM_005274215.2:c.673C= (BEST1) XP_005274272.1:p.Arg225=
XM_005274216.2:c.1014C= (BEST1) XP_005274273.1:p.Leu338=
XM_005274218.3:c.876C= (BEST1) XP_005274275.1:p.Leu292=
XM_005274219.2:c.867+1636C= (BEST1) XP_005274276.1:n.867+1636C=
XM_005274221.2:c.715-2321C= (BEST1) XP_005274278.1:n.715-2321C=
XM_011545229.1:c.991C= (BEST1) XP_011543531.1:p.Arg331=
XM_011545230.1:c.898C= (BEST1) XP_011543532.1:p.Arg300=
XM_011545231.1:c.673C= (BEST1) XP_011543533.1:p.Arg225=
XM_011545232.1:c.1194C= (BEST1) XP_011543534.1:p.Leu398=
XM_011545233.1:c.148C= (BEST1) XP_011543535.1:p.Arg50=
NM_001363591.1:c.673C= (BEST1) NP_001350520.1:p.Arg225=
NM_001363592.1:c.1194C= (BEST1) NP_001350521.1:p.Leu398=
NM_001363593.1:c.19C= (BEST1) NP_001350522.1:p.Arg7=
NR_134580.1:n.1774C= (BEST1)
XM_005274210.4:c.991C= (BEST1) XP_005274267.1:p.Arg331=
XM_005274215.4:c.673C= (BEST1) XP_005274272.1:p.Arg225=
XM_005274216.4:c.1014C= (BEST1) XP_005274273.1:p.Leu338=
XM_005274219.4:c.867+1636C= (BEST1) XP_005274276.1:n.867+1636C=
XM_005274221.4:c.715-2321C= (BEST1) XP_005274278.1:n.715-2321C=
XM_011545229.3:c.991C= (BEST1) XP_011543531.1:p.Arg331=
XM_011545230.3:c.898C= (BEST1) XP_011543532.1:p.Arg300=
XM_011545233.3:c.148C= (BEST1) XP_011543535.1:p.Arg50=
XM_017018230.2:c.876C= (BEST1) XP_016873719.1:p.Leu292=
XR_001747952.2:n.1692C= (BEST1)
XR_001747953.2:n.1557+1636C= (BEST1)
XR_001747954.2:n.1405-2321C= (BEST1)
NM_004183.4:c.991C= (BEST1) MANE Select NP_004174.1:p.Arg331=
NM_001139443.2:c.811C= (BEST1) NP_001132915.1:p.Arg271=
NM_001300786.2:c.730C= (BEST1) NP_001287715.1:p.Arg244=
NM_001300787.2:c.811C= (BEST1) NP_001287716.1:p.Arg271=
NM_001363591.2:c.673C= (BEST1) NP_001350520.1:p.Arg225=
NM_001363593.2:c.19C= (BEST1) NP_001350522.1:p.Arg7=
NR_134580.2:n.1307C= (BEST1)