Canonical Allele Identifier: CA213123327
Gene: BTRC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16405

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101553963_101553971del , CM000672.2:g.101553963_101553971del GRCh38
NC_000010.10:g.103313720_103313728del , CM000672.1:g.103313720_103313728del GRCh37
NC_000010.9:g.103303710_103303718del NCBI36
NG_009234.1:g.204896_204904del

Transcript Alleles

HGVS Amino-acid change
NM_001256856.1:c.*840_*848del VV NP_001243785.1:p.=
NM_003939.4:c.*840_*848del VV NP_003930.1:p.=
NM_033637.3:c.*840_*848del VV NP_378663.1:p.=
XM_005270264.2:c.*840_*848del XP_005270321.1:p.=
XM_006718054.2:c.*840_*848del XP_006718117.1:p.=
XM_011540320.1:c.*840_*848del XP_011538622.1:p.=
XM_011540320.2:c.*840_*848del
XM_017016870.1:c.*840_*848del XP_016872359.1:p.=
XM_017016871.1:c.*840_*848del XP_016872360.1:p.=
XM_017016872.1:c.*840_*848del XP_016872361.1:p.=
XM_017016873.2:c.*840_*848del XP_016872362.1:p.=
XM_017016874.1:c.*840_*848del XP_016872363.1:p.=
XM_024448246.1:c.*840_*848del XP_024304014.1:p.=
XM_024448247.1:c.*840_*848del XP_024304015.1:p.=
XR_001747256.1:n.3009_3017del
NM_033637.4:c.*840_*848del VV MANE Preferred
ENST00000370187.7:c.*840_*848del ENSP00000359206.3:p.=
ENST00000393441.8:c.*840_*848del ENSP00000377088.5:p.=
ENST00000408038.6:c.*840_*848del ENSP00000385339.2:p.=