Canonical Allele Identifier: CA337230829
Gene: BCAP31 HGNC NCBI

Linked Data

dbSNP Id: rs112882943

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153720871C>G , CM000685.2:g.153720871C>G GRCh38
NC_000023.10:g.152986326C>G , CM000685.1:g.152986326C>G GRCh37
NC_000023.9:g.152639520C>G NCBI36
NG_009022.2:g.1004C>G
NG_023231.1:g.8876G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000345046.12:c.193+1G>C MANE Select ENSP00000343458.6:n.193+1G>C
ENST00000458587.8:c.394+1G>C ENSP00000392330.2:n.394+1G>C
ENST00000645377.1:c.193+1G>C ENSP00000494936.1:n.193+1G>C
ENST00000645802.1:n.300+1G>C
ENST00000647529.1:c.193+1G>C ENSP00000494052.1:n.193+1G>C
ENST00000672675.1:c.193+1G>C ENSP00000499882.1:n.193+1G>C
ENST00000345046.10:c.193+1G>C ENSP00000343458.6:n.193+1G>C
ENST00000416815.5:c.193+1G>C ENSP00000394270.1:n.193+1G>C
ENST00000423827.5:c.193+1G>C ENSP00000389740.1:n.193+1G>C
ENST00000429550.5:c.193+1G>C ENSP00000409888.1:n.193+1G>C
ENST00000430088.1:c.193+1G>C ENSP00000402342.1:n.193+1G>C
ENST00000442093.5:c.193+1G>C ENSP00000400345.1:n.193+1G>C
ENST00000458587.6:c.394+1G>C ENSP00000392330.2:n.394+1G>C
ENST00000468947.1:n.286+1G>C
NM_001139441.1:c.193+1G>C NP_001132913.1:n.193+1G>C
NM_001139457.2:c.394+1G>C NP_001132929.1:n.394+1G>C
NM_001256447.1:c.193+1G>C NP_001243376.1:n.193+1G>C
NM_005745.7:c.193+1G>C NP_005736.3:n.193+1G>C
XR_002958758.1:n.824+1G>C
XR_002958759.1:n.650+1G>C
XR_002958760.1:n.415+1G>C
XR_002958761.1:n.349+1G>C
NM_001256447.2:c.193+1G>C MANE Select NP_001243376.1:n.193+1G>C
NM_005745.8:c.193+1G>C NP_005736.3:n.193+1G>C