Canonical Allele Identifier: CA1138538645
Gene: BCAP31 HGNC NCBI

Linked Data

dbSNP Id: rs1557051536

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153723491G>A , CM000685.2:g.153723491G>A GRCh38
NC_000023.10:g.152988946G>A , CM000685.1:g.152988946G>A GRCh37
NC_000023.9:g.152642140G>A NCBI36
NG_009022.2:g.3624G>A
NG_023231.1:g.6256C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000345046.12:c.-44-203C>T MANE Select ENSP00000343458.6:n.-44-203C>T
ENST00000458587.8:c.157+17C>T ENSP00000392330.2:n.157+17C>T
ENST00000645377.1:c.-44-203C>T ENSP00000494936.1:n.-44-203C>T
ENST00000645802.1:n.64-203C>T
ENST00000647529.1:c.-45+17C>T ENSP00000494052.1:n.-45+17C>T
ENST00000672675.1:c.-44-203C>T ENSP00000499882.1:n.-44-203C>T
ENST00000345046.10:c.-44-203C>T ENSP00000343458.6:n.-44-203C>T
ENST00000416815.5:c.-44-203C>T ENSP00000394270.1:n.-44-203C>T
ENST00000423827.5:c.-44-203C>T ENSP00000389740.1:n.-44-203C>T
ENST00000429550.5:c.-44-203C>T ENSP00000409888.1:n.-44-203C>T
ENST00000442093.5:c.-44-203C>T ENSP00000400345.1:n.-44-203C>T
ENST00000458587.6:c.157+17C>T ENSP00000392330.2:n.157+17C>T
NM_001139441.1:c.-44-203C>T NP_001132913.1:n.-44-203C>T
NM_001139457.2:c.157+17C>T NP_001132929.1:n.157+17C>T
NM_001256447.1:c.-44-203C>T NP_001243376.1:n.-44-203C>T
NM_005745.7:c.-44-203C>T NP_005736.3:n.-44-203C>T
XR_002958758.1:n.587+17C>T
XR_002958759.1:n.414-203C>T
XR_002958760.1:n.179-203C>T
XR_002958761.1:n.113-203C>T
NM_001256447.2:c.-44-203C>T MANE Select NP_001243376.1:n.-44-203C>T
NM_005745.8:c.-44-203C>T NP_005736.3:n.-44-203C>T