Canonical Allele Identifier: CA2695041825

Gene: BCAP31

Linked Data

• gnomAD v4: X-153723381-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153723382dup , CM000685.2:g.153723382dup	GRCh38
NC_000023.10:g.152988837dup , CM000685.1:g.152988837dup	GRCh37
NC_000023.9:g.152642031dup	NCBI36
NG_009022.2:g.3515dup
NG_023231.1:g.6365dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345046.12:c.-44-94dup MANE Select	ENSP00000343458.6:n.-44-94dup
ENST00000458587.8:c.158-94dup	ENSP00000392330.2:n.158-94dup
ENST00000645377.1:c.-44-94dup	ENSP00000494936.1:n.-44-94dup
ENST00000645802.1:n.64-94dup
ENST00000647529.1:c.-44-94dup	ENSP00000494052.1:n.-44-94dup
ENST00000672675.1:c.-44-94dup	ENSP00000499882.1:n.-44-94dup
ENST00000345046.10:c.-44-94dup	ENSP00000343458.6:n.-44-94dup
ENST00000416815.5:c.-44-94dup	ENSP00000394270.1:n.-44-94dup
ENST00000423827.5:c.-44-94dup	ENSP00000389740.1:n.-44-94dup
ENST00000429550.5:c.-44-94dup	ENSP00000409888.1:n.-44-94dup
ENST00000430088.1:c.-138dup	ENSP00000402342.1:n.-138dup
ENST00000442093.5:c.-44-94dup	ENSP00000400345.1:n.-44-94dup
ENST00000458587.6:c.158-94dup	ENSP00000392330.2:n.158-94dup
NM_001139441.1:c.-44-94dup	NP_001132913.1:n.-44-94dup
NM_001139457.2:c.158-94dup	NP_001132929.1:n.158-94dup
NM_001256447.1:c.-44-94dup	NP_001243376.1:n.-44-94dup
NM_005745.7:c.-44-94dup	NP_005736.3:n.-44-94dup
XR_002958758.1:n.588-94dup
XR_002958759.1:n.414-94dup
XR_002958760.1:n.179-94dup
XR_002958761.1:n.113-94dup
NM_001256447.2:c.-44-94dup MANE Select	NP_001243376.1:n.-44-94dup
NM_005745.8:c.-44-94dup	NP_005736.3:n.-44-94dup