Canonical Allele Identifier: CA415094970

Gene: BCAP31

Linked Data

• MyVariant Identifiers: chrX:g.152986332A>T (hg19) ; chrX:g.153720877A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153720877A>T , CM000685.2:g.153720877A>T	GRCh38
NC_000023.10:g.152986332A>T , CM000685.1:g.152986332A>T	GRCh37
NC_000023.9:g.152639526A>T	NCBI36
NG_009022.2:g.1010A>T
NG_023231.1:g.8870T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000345046.12:c.188T>A MANE Select	ENSP00000343458.6:p.Val63Asp
ENST00000458587.8:c.389T>A	ENSP00000392330.2:p.Val130Asp
ENST00000645377.1:c.188T>A	ENSP00000494936.1:p.Val63Asp
ENST00000645802.1:n.295T>A
ENST00000647529.1:c.188T>A	ENSP00000494052.1:p.Val63Asp
ENST00000672675.1:c.188T>A	ENSP00000499882.1:p.Val63Asp
ENST00000345046.10:c.188T>A	ENSP00000343458.6:p.Val63Asp
ENST00000416815.5:c.188T>A	ENSP00000394270.1:p.Val63Asp
ENST00000423827.5:c.188T>A	ENSP00000389740.1:p.Val63Asp
ENST00000429550.5:c.188T>A	ENSP00000409888.1:p.Val63Asp
ENST00000430088.1:c.188T>A	ENSP00000402342.1:p.Val63Asp
ENST00000442093.5:c.188T>A	ENSP00000400345.1:p.Val63Asp
ENST00000458587.6:c.389T>A	ENSP00000392330.2:p.Val130Asp
ENST00000468947.1:n.281T>A
NM_001139441.1:c.188T>A	NP_001132913.1:p.Val63Asp
NM_001139457.2:c.389T>A	NP_001132929.1:p.Val130Asp
NM_001256447.1:c.188T>A	NP_001243376.1:p.Val63Asp
NM_005745.7:c.188T>A	NP_005736.3:p.Val63Asp
XR_002958758.1:n.819T>A
XR_002958759.1:n.645T>A
XR_002958760.1:n.410T>A
XR_002958761.1:n.344T>A
NM_001256447.2:c.188T>A MANE Select	NP_001243376.1:p.Val63Asp
NM_005745.8:c.188T>A	NP_005736.3:p.Val63Asp