Canonical Allele Identifier: CA519205857

Gene: BCAP31

Linked Data

• MyVariant Identifiers: chrX:g.152986336A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153720881A>G , CM000685.2:g.153720881A>G	GRCh38
NC_000023.10:g.152986336A>G , CM000685.1:g.152986336A>G	GRCh37
NC_000023.9:g.152639530A>G	NCBI36
NG_009022.2:g.1014A>G
NG_023231.1:g.8866T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345046.12:c.184T>C MANE Select	ENSP00000343458.6:p.Leu62=
ENST00000458587.8:c.385T>C	ENSP00000392330.2:p.Leu129=
ENST00000645377.1:c.184T>C	ENSP00000494936.1:p.Leu62=
ENST00000645802.1:n.291T>C
ENST00000647529.1:c.184T>C	ENSP00000494052.1:p.Leu62=
ENST00000672675.1:c.184T>C	ENSP00000499882.1:p.Leu62=
ENST00000345046.10:c.184T>C	ENSP00000343458.6:p.Leu62=
ENST00000416815.5:c.184T>C	ENSP00000394270.1:p.Leu62=
ENST00000423827.5:c.184T>C	ENSP00000389740.1:p.Leu62=
ENST00000429550.5:c.184T>C	ENSP00000409888.1:p.Leu62=
ENST00000430088.1:c.184T>C	ENSP00000402342.1:p.Leu62=
ENST00000442093.5:c.184T>C	ENSP00000400345.1:p.Leu62=
ENST00000458587.6:c.385T>C	ENSP00000392330.2:p.Leu129=
ENST00000468947.1:n.277T>C
NM_001139441.1:c.184T>C	NP_001132913.1:p.Leu62=
NM_001139457.2:c.385T>C	NP_001132929.1:p.Leu129=
NM_001256447.1:c.184T>C	NP_001243376.1:p.Leu62=
NM_005745.7:c.184T>C	NP_005736.3:p.Leu62=
XR_002958758.1:n.815T>C
XR_002958759.1:n.641T>C
XR_002958760.1:n.406T>C
XR_002958761.1:n.340T>C
NM_001256447.2:c.184T>C MANE Select	NP_001243376.1:p.Leu62=
NM_005745.8:c.184T>C	NP_005736.3:p.Leu62=