Canonical Allele Identifier: CA873268993

Gene: BCAP31

Linked Data

• dbSNP Id: rs1179685575
• gnomAD v3: X-153723499-G-A
• gnomAD v4: X-153723499-G-A
• MyVariant Identifiers: chrX:g.153723499G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153723499G>A , CM000685.2:g.153723499G>A	GRCh38
NC_000023.10:g.152988954G>A , CM000685.1:g.152988954G>A	GRCh37
NC_000023.9:g.152642148G>A	NCBI36
NG_009022.2:g.3632G>A
NG_023231.1:g.6248C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345046.12:c.-44-211C>T MANE Select	ENSP00000343458.6:n.-44-211C>T
ENST00000458587.8:c.157+9C>T	ENSP00000392330.2:n.157+9C>T
ENST00000645377.1:c.-44-211C>T	ENSP00000494936.1:n.-44-211C>T
ENST00000645802.1:n.64-211C>T
ENST00000647529.1:c.-45+9C>T	ENSP00000494052.1:n.-45+9C>T
ENST00000672675.1:c.-44-211C>T	ENSP00000499882.1:n.-44-211C>T
ENST00000345046.10:c.-44-211C>T	ENSP00000343458.6:n.-44-211C>T
ENST00000416815.5:c.-44-211C>T	ENSP00000394270.1:n.-44-211C>T
ENST00000423827.5:c.-44-211C>T	ENSP00000389740.1:n.-44-211C>T
ENST00000429550.5:c.-44-211C>T	ENSP00000409888.1:n.-44-211C>T
ENST00000442093.5:c.-44-211C>T	ENSP00000400345.1:n.-44-211C>T
ENST00000458587.6:c.157+9C>T	ENSP00000392330.2:n.157+9C>T
NM_001139441.1:c.-44-211C>T	NP_001132913.1:n.-44-211C>T
NM_001139457.2:c.157+9C>T	NP_001132929.1:n.157+9C>T
NM_001256447.1:c.-44-211C>T	NP_001243376.1:n.-44-211C>T
NM_005745.7:c.-44-211C>T	NP_005736.3:n.-44-211C>T
XR_002958758.1:n.587+9C>T
XR_002958759.1:n.414-211C>T
XR_002958760.1:n.179-211C>T
XR_002958761.1:n.113-211C>T
NM_001256447.2:c.-44-211C>T MANE Select	NP_001243376.1:n.-44-211C>T
NM_005745.8:c.-44-211C>T	NP_005736.3:n.-44-211C>T