Canonical Allele Identifier: CA415096697

Gene: BCAP31

Linked Data

• MyVariant Identifiers: chrX:g.152989018C>A (hg19) ; chrX:g.153723563C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153723563C>A , CM000685.2:g.153723563C>A	GRCh38
NC_000023.10:g.152989018C>A , CM000685.1:g.152989018C>A	GRCh37
NC_000023.9:g.152642212C>A	NCBI36
NG_009022.2:g.3696C>A
NG_023231.1:g.6184G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345046.12:c.-44-275G>T MANE Select	ENSP00000343458.6:n.-44-275G>T
ENST00000458587.8:c.102G>T	ENSP00000392330.2:p.Gln34His
ENST00000645377.1:c.-44-275G>T	ENSP00000494936.1:n.-44-275G>T
ENST00000645802.1:n.64-275G>T
ENST00000647529.1:c.-100G>T	ENSP00000494052.1:n.-100G>T
ENST00000672675.1:c.-44-275G>T	ENSP00000499882.1:n.-44-275G>T
ENST00000345046.10:c.-44-275G>T	ENSP00000343458.6:n.-44-275G>T
ENST00000416815.5:c.-44-275G>T	ENSP00000394270.1:n.-44-275G>T
ENST00000423827.5:c.-44-275G>T	ENSP00000389740.1:n.-44-275G>T
ENST00000429550.5:c.-44-275G>T	ENSP00000409888.1:n.-44-275G>T
ENST00000442093.5:c.-44-275G>T	ENSP00000400345.1:n.-44-275G>T
ENST00000458587.6:c.102G>T	ENSP00000392330.2:p.Gln34His
NM_001139441.1:c.-44-275G>T	NP_001132913.1:n.-44-275G>T
NM_001139457.2:c.102G>T	NP_001132929.1:p.Gln34His
NM_001256447.1:c.-44-275G>T	NP_001243376.1:n.-44-275G>T
NM_005745.7:c.-44-275G>T	NP_005736.3:n.-44-275G>T
XR_002958758.1:n.532G>T
XR_002958759.1:n.414-275G>T
XR_002958760.1:n.179-275G>T
XR_002958761.1:n.113-275G>T
NM_001256447.2:c.-44-275G>T MANE Select	NP_001243376.1:n.-44-275G>T
NM_005745.8:c.-44-275G>T	NP_005736.3:n.-44-275G>T