Canonical Allele Identifier: CA2580612123

Gene: BCAP31

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153716860_153722609del , CM000685.2:g.153716860_153722609del	GRCh38
NC_000023.10:g.152982315_152988064del , CM000685.1:g.152982315_152988064del	GRCh37
NC_000023.9:g.152635509_152641258del	NCBI36
NG_023231.1:g.7139_12888del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345046.12:c.92+545_194-1170del
ENST00000458587.8:c.293+545_395-1170del
ENST00000645377.1:c.92+545_194-1170del
ENST00000645802.1:n.199+545_301-1170del
ENST00000647529.1:c.92+545_194-1170del
ENST00000672675.1:c.92+545_194-1170del
ENST00000345046.10:c.92+545_194-1170del
ENST00000416815.5:c.92+545_194-1170del
ENST00000423827.5:c.92+545_194-1170del
ENST00000429550.5:c.92+545_194-1170del
ENST00000430088.1:c.92+545_194-1170del
ENST00000442093.5:c.92+545_194-1170del
ENST00000458587.6:c.293+545_395-1170del
NM_001139441.1:c.92+545_194-1170del
NM_001139457.2:c.293+545_395-1170del
NM_001256447.1:c.92+545_194-1170del
NM_005745.7:c.92+545_194-1170del
XR_002958758.1:n.723+545_825-1170del
XR_002958759.1:n.549+545_651-1170del
XR_002958760.1:n.314+545_416-1170del
XR_002958761.1:n.248+545_350-1170del
NM_001256447.2:c.92+545_194-1170del
NM_005745.8:c.92+545_194-1170del