Canonical Allele Identifier: CA337399115
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs3906
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19562813_19562814delinsTTGTACAGAGA , CM000686.2:g.19562813_19562814delinsTTGTACAGAGA GRCh38
NC_000024.9:g.21724699_21724700delinsTTGTACAGAGA , CM000686.1:g.21724699_21724700delinsTTGTACAGAGA GRCh37
NC_000024.8:g.20184087_20184088delinsTTGTACAGAGA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000693243.1:n.26+4168_26+4169delinsTCTCTGTACAA
ENST00000650676.1:n.111+4168_111+4169delinsTCTCTGTACAA
ENST00000651484.1:n.70+4168_70+4169delinsTCTCTGTACAA
XR_938626.1:n.741_742delinsTCTCTGTACAA
XR_938627.1:n.741_742delinsTCTCTGTACAA
XR_938628.1:n.270+4168_270+4169delinsTCTCTGTACAA
XR_938629.1:n.741_742delinsTCTCTGTACAA
XR_001756064.2:n.198+4168_198+4169delinsTCTCTGTACAA
XR_001756065.1:n.198+4168_198+4169delinsTCTCTGTACAA
XR_001756066.1:n.199-3395_199-3394delinsTCTCTGTACAA
XR_938626.2:n.1137_1138delinsTCTCTGTACAA
XR_938627.2:n.1137_1138delinsTCTCTGTACAA
XR_938628.3:n.198+4168_198+4169delinsTCTCTGTACAA
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