Canonical Allele Identifier: CA415095324

Gene: BCAP31

Linked Data

• COSMIC: COSM755759 ; COSM1151543
• MyVariant Identifiers: chrX:g.152986426A>G (hg19) ; chrX:g.153720971A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153720971A>G , CM000685.2:g.153720971A>G	GRCh38
NC_000023.10:g.152986426A>G , CM000685.1:g.152986426A>G	GRCh37
NC_000023.9:g.152639620A>G	NCBI36
NG_009022.2:g.1104A>G
NG_023231.1:g.8776T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345046.12:c.94T>C MANE Select	ENSP00000343458.6:p.Trp32Arg
ENST00000458587.8:c.295T>C	ENSP00000392330.2:p.Trp99Arg
ENST00000645377.1:c.94T>C	ENSP00000494936.1:p.Trp32Arg
ENST00000645802.1:n.201T>C
ENST00000647529.1:c.94T>C	ENSP00000494052.1:p.Trp32Arg
ENST00000672675.1:c.94T>C	ENSP00000499882.1:p.Trp32Arg
ENST00000345046.10:c.94T>C	ENSP00000343458.6:p.Trp32Arg
ENST00000416815.5:c.94T>C	ENSP00000394270.1:p.Trp32Arg
ENST00000423827.5:c.94T>C	ENSP00000389740.1:p.Trp32Arg
ENST00000429550.5:c.94T>C	ENSP00000409888.1:p.Trp32Arg
ENST00000430088.1:c.94T>C	ENSP00000402342.1:p.Trp32Arg
ENST00000442093.5:c.94T>C	ENSP00000400345.1:p.Trp32Arg
ENST00000458587.6:c.295T>C	ENSP00000392330.2:p.Trp99Arg
ENST00000468947.1:n.187T>C
NM_001139441.1:c.94T>C	NP_001132913.1:p.Trp32Arg
NM_001139457.2:c.295T>C	NP_001132929.1:p.Trp99Arg
NM_001256447.1:c.94T>C	NP_001243376.1:p.Trp32Arg
NM_005745.7:c.94T>C	NP_005736.3:p.Trp32Arg
XR_002958758.1:n.725T>C
XR_002958759.1:n.551T>C
XR_002958760.1:n.316T>C
XR_002958761.1:n.250T>C
NM_001256447.2:c.94T>C MANE Select	NP_001243376.1:p.Trp32Arg
NM_005745.8:c.94T>C	NP_005736.3:p.Trp32Arg