Canonical Allele Identifier: CA1932270695
Gene: BTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101553882G= , CM000672.2:g.101553882G= GRCh38
NC_000010.10:g.103313639G= , CM000672.1:g.103313639G= GRCh37
NC_000010.9:g.103303629G= NCBI36
NG_009234.1:g.204815G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370187.8:c.*759G= MANE Select ENSP00000359206.3:n.*759G=
ENST00000370187.7:c.*759G= ENSP00000359206.3:n.*759G=
ENST00000393441.8:c.*759G= ENSP00000377088.5:n.*759G=
ENST00000408038.6:c.*759G= ENSP00000385339.2:n.*759G=
NM_001256856.1:c.*759G= NP_001243785.1:n.*759G=
NM_003939.4:c.*759G= NP_003930.1:n.*759G=
NM_033637.3:c.*759G= NP_378663.1:n.*759G=
XM_005270264.2:c.*759G= XP_005270321.1:n.*759G=
XM_006718054.2:c.*759G= XP_006718117.1:n.*759G=
XM_011540320.1:c.*759G= XP_011538622.1:n.*759G=
XM_011540320.2:c.*759G= XP_011538622.1:n.*759G=
XM_017016870.1:c.*759G= XP_016872359.1:n.*759G=
XM_017016871.1:c.*759G= XP_016872360.1:n.*759G=
XM_017016872.1:c.*759G= XP_016872361.1:n.*759G=
XM_017016873.2:c.*759G= XP_016872362.1:n.*759G=
XM_017016874.1:c.*759G= XP_016872363.1:n.*759G=
XM_024448246.1:c.*759G= XP_024304014.1:n.*759G=
XM_024448247.1:c.*759G= XP_024304015.1:n.*759G=
XR_001747256.1:n.2928G=
NM_033637.4:c.*759G= MANE Select NP_378663.1:n.*759G=
NM_003939.5:c.*759G= NP_003930.1:n.*759G=
NM_001256856.2:c.*759G= NP_001243785.1:n.*759G=