Canonical Allele Identifier: CA2695041789
Gene: BCAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153723342_153723351del , CM000685.2:g.153723342_153723351del GRCh38
NC_000023.10:g.152988797_152988806del , CM000685.1:g.152988797_152988806del GRCh37
NC_000023.9:g.152641991_152642000del NCBI36
NG_009022.2:g.3475_3484del
NG_023231.1:g.6397_6406del

Transcript Alleles

HGVS Amino-acid Change
ENST00000345046.12:c.-44-62_-44-53del MANE Select ENSP00000343458.6:n.-44-62_-44-53del
ENST00000458587.8:c.158-62_158-53del ENSP00000392330.2:n.158-62_158-53del
ENST00000645377.1:c.-44-62_-44-53del ENSP00000494936.1:n.-44-62_-44-53del
ENST00000645802.1:n.64-62_64-53del
ENST00000647529.1:c.-44-62_-44-53del ENSP00000494052.1:n.-44-62_-44-53del
ENST00000672675.1:c.-44-62_-44-53del ENSP00000499882.1:n.-44-62_-44-53del
ENST00000345046.10:c.-44-62_-44-53del ENSP00000343458.6:n.-44-62_-44-53del
ENST00000416815.5:c.-44-62_-44-53del ENSP00000394270.1:n.-44-62_-44-53del
ENST00000423827.5:c.-44-62_-44-53del ENSP00000389740.1:n.-44-62_-44-53del
ENST00000429550.5:c.-44-62_-44-53del ENSP00000409888.1:n.-44-62_-44-53del
ENST00000430088.1:c.-106_-97del ENSP00000402342.1:n.-106_-97del
ENST00000442093.5:c.-44-62_-44-53del ENSP00000400345.1:n.-44-62_-44-53del
ENST00000458587.6:c.158-62_158-53del ENSP00000392330.2:n.158-62_158-53del
NM_001139441.1:c.-44-62_-44-53del NP_001132913.1:n.-44-62_-44-53del
NM_001139457.2:c.158-62_158-53del NP_001132929.1:n.158-62_158-53del
NM_001256447.1:c.-44-62_-44-53del NP_001243376.1:n.-44-62_-44-53del
NM_005745.7:c.-44-62_-44-53del NP_005736.3:n.-44-62_-44-53del
XR_002958758.1:n.588-62_588-53del
XR_002958759.1:n.414-62_414-53del
XR_002958760.1:n.179-62_179-53del
XR_002958761.1:n.113-62_113-53del
NM_001256447.2:c.-44-62_-44-53del MANE Select NP_001243376.1:n.-44-62_-44-53del
NM_005745.8:c.-44-62_-44-53del NP_005736.3:n.-44-62_-44-53del