Canonical Allele Identifier: CA8018059
Gene: HSD3B7 HGNC NCBI

Linked Data

dbSNP Id: rs746191063

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30986953del , CM000678.2:g.30986953del GRCh38
NC_000016.9:g.30998274del , CM000678.1:g.30998274del GRCh37
NC_000016.8:g.30905775del NCBI36
NG_012346.1:g.6756del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297679.10:c.645del MANE Select ENSP00000297679.5:p.Trp215CysfsTer?
ENST00000262520.10:c.531+249del ENSP00000262520.6:n.531+249del
ENST00000297679.9:c.645del ENSP00000297679.5:p.Trp215CysfsTer?
NM_001142777.1:c.531+249del NP_001136249.1:n.531+249del
NM_001142778.1:c.531+249del NP_001136250.1:n.531+249del
NM_025193.3:c.645del NP_079469.2:p.Trp215CysfsTer?
XM_005255601.3:c.645del XP_005255658.2:p.Trp215CysfsTer?
XM_011545960.1:c.645del XP_011544262.1:p.Trp215CysfsTer?
XM_011545961.1:c.645del XP_011544263.1:p.Trp215CysfsTer?
XM_011545962.1:c.531+249del XP_011544264.1:n.531+249del
XM_011545960.2:c.645del XP_011544262.1:p.Trp215CysfsTer?
XM_011545962.2:c.531+249del XP_011544264.1:n.531+249del
XM_017023732.1:c.531+249del XP_016879221.1:n.531+249del
NM_025193.4:c.645del MANE Select NP_079469.2:p.Trp215CysfsTer?
NM_001142777.2:c.531+249del NP_001136249.1:n.531+249del
NM_001142778.2:c.531+249del NP_001136250.1:n.531+249del