Canonical Allele Identifier: CA2466448821
Gene: BCAP31 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153720873G= , CM000685.2:g.153720873G= GRCh38
NC_000023.10:g.152986328G= , CM000685.1:g.152986328G= GRCh37
NC_000023.9:g.152639522G= NCBI36
NG_009022.2:g.1006G=
NG_023231.1:g.8874C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000345046.12:c.192C= MANE Select ENSP00000343458.6:p.Ile64=
ENST00000458587.8:c.393C= ENSP00000392330.2:p.Ile131=
ENST00000645377.1:c.192C= ENSP00000494936.1:p.Ile64=
ENST00000645802.1:n.299C=
ENST00000647529.1:c.192C= ENSP00000494052.1:p.Ile64=
ENST00000672675.1:c.192C= ENSP00000499882.1:p.Ile64=
ENST00000345046.10:c.192C= ENSP00000343458.6:p.Ile64=
ENST00000416815.5:c.192C= ENSP00000394270.1:p.Ile64=
ENST00000423827.5:c.192C= ENSP00000389740.1:p.Ile64=
ENST00000429550.5:c.192C= ENSP00000409888.1:p.Ile64=
ENST00000430088.1:c.192C= ENSP00000402342.1:p.Ile64=
ENST00000442093.5:c.192C= ENSP00000400345.1:p.Ile64=
ENST00000458587.6:c.393C= ENSP00000392330.2:p.Ile131=
ENST00000468947.1:n.285C=
NM_001139441.1:c.192C= NP_001132913.1:p.Ile64=
NM_001139457.2:c.393C= NP_001132929.1:p.Ile131=
NM_001256447.1:c.192C= NP_001243376.1:p.Ile64=
NM_005745.7:c.192C= NP_005736.3:p.Ile64=
XR_002958758.1:n.823C=
XR_002958759.1:n.649C=
XR_002958760.1:n.414C=
XR_002958761.1:n.348C=
NM_001256447.2:c.192C= MANE Select NP_001243376.1:p.Ile64=
NM_005745.8:c.192C= NP_005736.3:p.Ile64=