Canonical Allele Identifier: CA415096562
Gene: BCAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153723525T>C , CM000685.2:g.153723525T>C GRCh38
NC_000023.10:g.152988980T>C , CM000685.1:g.152988980T>C GRCh37
NC_000023.9:g.152642174T>C NCBI36
NG_009022.2:g.3658T>C
NG_023231.1:g.6222A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000345046.12:c.-44-237A>G MANE Select ENSP00000343458.6:n.-44-237A>G
ENST00000458587.8:c.140A>G ENSP00000392330.2:p.His47Arg
ENST00000645377.1:c.-44-237A>G ENSP00000494936.1:n.-44-237A>G
ENST00000645802.1:n.64-237A>G
ENST00000647529.1:c.-62A>G ENSP00000494052.1:n.-62A>G
ENST00000672675.1:c.-44-237A>G ENSP00000499882.1:n.-44-237A>G
ENST00000345046.10:c.-44-237A>G ENSP00000343458.6:n.-44-237A>G
ENST00000416815.5:c.-44-237A>G ENSP00000394270.1:n.-44-237A>G
ENST00000423827.5:c.-44-237A>G ENSP00000389740.1:n.-44-237A>G
ENST00000429550.5:c.-44-237A>G ENSP00000409888.1:n.-44-237A>G
ENST00000442093.5:c.-44-237A>G ENSP00000400345.1:n.-44-237A>G
ENST00000458587.6:c.140A>G ENSP00000392330.2:p.His47Arg
NM_001139441.1:c.-44-237A>G NP_001132913.1:n.-44-237A>G
NM_001139457.2:c.140A>G NP_001132929.1:p.His47Arg
NM_001256447.1:c.-44-237A>G NP_001243376.1:n.-44-237A>G
NM_005745.7:c.-44-237A>G NP_005736.3:n.-44-237A>G
XR_002958758.1:n.570A>G
XR_002958759.1:n.414-237A>G
XR_002958760.1:n.179-237A>G
XR_002958761.1:n.113-237A>G
NM_001256447.2:c.-44-237A>G MANE Select NP_001243376.1:n.-44-237A>G
NM_005745.8:c.-44-237A>G NP_005736.3:n.-44-237A>G