Canonical Allele Identifier: CA519209662

Gene: BCAP31

Linked Data

• MyVariant Identifiers: chrX:g.152989024C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153723569C>A , CM000685.2:g.153723569C>A	GRCh38
NC_000023.10:g.152989024C>A , CM000685.1:g.152989024C>A	GRCh37
NC_000023.9:g.152642218C>A	NCBI36
NG_009022.2:g.3702C>A
NG_023231.1:g.6178G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345046.12:c.-44-281G>T MANE Select	ENSP00000343458.6:n.-44-281G>T
ENST00000458587.8:c.96G>T	ENSP00000392330.2:p.Leu32=
ENST00000645377.1:c.-44-281G>T	ENSP00000494936.1:n.-44-281G>T
ENST00000645802.1:n.64-281G>T
ENST00000647529.1:c.-106G>T	ENSP00000494052.1:n.-106G>T
ENST00000672675.1:c.-44-281G>T	ENSP00000499882.1:n.-44-281G>T
ENST00000345046.10:c.-44-281G>T	ENSP00000343458.6:n.-44-281G>T
ENST00000416815.5:c.-44-281G>T	ENSP00000394270.1:n.-44-281G>T
ENST00000423827.5:c.-44-281G>T	ENSP00000389740.1:n.-44-281G>T
ENST00000429550.5:c.-44-281G>T	ENSP00000409888.1:n.-44-281G>T
ENST00000442093.5:c.-44-281G>T	ENSP00000400345.1:n.-44-281G>T
ENST00000458587.6:c.96G>T	ENSP00000392330.2:p.Leu32=
NM_001139441.1:c.-44-281G>T	NP_001132913.1:n.-44-281G>T
NM_001139457.2:c.96G>T	NP_001132929.1:p.Leu32=
NM_001256447.1:c.-44-281G>T	NP_001243376.1:n.-44-281G>T
NM_005745.7:c.-44-281G>T	NP_005736.3:n.-44-281G>T
XR_002958758.1:n.526G>T
XR_002958759.1:n.414-281G>T
XR_002958760.1:n.179-281G>T
XR_002958761.1:n.113-281G>T
NM_001256447.2:c.-44-281G>T MANE Select	NP_001243376.1:n.-44-281G>T
NM_005745.8:c.-44-281G>T	NP_005736.3:n.-44-281G>T