Canonical Allele Identifier: CA415094955

Gene: BCAP31

Linked Data

• MyVariant Identifiers: chrX:g.152986328G>C (hg19) ; chrX:g.153720873G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153720873G>C , CM000685.2:g.153720873G>C	GRCh38
NC_000023.10:g.152986328G>C , CM000685.1:g.152986328G>C	GRCh37
NC_000023.9:g.152639522G>C	NCBI36
NG_009022.2:g.1006G>C
NG_023231.1:g.8874C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000345046.12:c.192C>G MANE Select	ENSP00000343458.6:p.Ile64Met
ENST00000458587.8:c.393C>G	ENSP00000392330.2:p.Ile131Met
ENST00000645377.1:c.192C>G	ENSP00000494936.1:p.Ile64Met
ENST00000645802.1:n.299C>G
ENST00000647529.1:c.192C>G	ENSP00000494052.1:p.Ile64Met
ENST00000672675.1:c.192C>G	ENSP00000499882.1:p.Ile64Met
ENST00000345046.10:c.192C>G	ENSP00000343458.6:p.Ile64Met
ENST00000416815.5:c.192C>G	ENSP00000394270.1:p.Ile64Met
ENST00000423827.5:c.192C>G	ENSP00000389740.1:p.Ile64Met
ENST00000429550.5:c.192C>G	ENSP00000409888.1:p.Ile64Met
ENST00000430088.1:c.192C>G	ENSP00000402342.1:p.Ile64Met
ENST00000442093.5:c.192C>G	ENSP00000400345.1:p.Ile64Met
ENST00000458587.6:c.393C>G	ENSP00000392330.2:p.Ile131Met
ENST00000468947.1:n.285C>G
NM_001139441.1:c.192C>G	NP_001132913.1:p.Ile64Met
NM_001139457.2:c.393C>G	NP_001132929.1:p.Ile131Met
NM_001256447.1:c.192C>G	NP_001243376.1:p.Ile64Met
NM_005745.7:c.192C>G	NP_005736.3:p.Ile64Met
XR_002958758.1:n.823C>G
XR_002958759.1:n.649C>G
XR_002958760.1:n.414C>G
XR_002958761.1:n.348C>G
NM_001256447.2:c.192C>G MANE Select	NP_001243376.1:p.Ile64Met
NM_005745.8:c.192C>G	NP_005736.3:p.Ile64Met