Canonical Allele Identifier: CA2632795779
Gene: HSD3B7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30987858_30987871del , CM000678.2:g.30987858_30987871del GRCh38
NC_000016.9:g.30999179_30999192del , CM000678.1:g.30999179_30999192del GRCh37
NC_000016.8:g.30906680_30906693del NCBI36
NG_012346.1:g.7661_7674del
NG_041829.1:g.27639_27652del

Transcript Alleles

HGVS Amino-acid Change
ENST00000297679.10:c.785_798del MANE Select ENSP00000297679.5:p.Gly262GlufsTer?
ENST00000262520.10:c.*31_*44del ENSP00000262520.6:n.*31_*44del
ENST00000297679.9:c.785_798del ENSP00000297679.5:p.Gly262GlufsTer?
NM_001142777.1:c.*31_*44del NP_001136249.1:n.*31_*44del
NM_001142778.1:c.*31_*44del NP_001136250.1:n.*31_*44del
NM_025193.3:c.785_798del NP_079469.2:p.Gly262GlufsTer?
XM_005255601.3:c.785_798del XP_005255658.2:p.Gly262GlufsTer?
XM_011545960.1:c.785_798del XP_011544262.1:p.Gly262GlufsTer?
XM_011545961.1:c.785_798del XP_011544263.1:p.Gly262GlufsTer?
XM_011545962.1:c.*31_*44del XP_011544264.1:n.*31_*44del
XM_011545960.2:c.785_798del XP_011544262.1:p.Gly262GlufsTer?
XM_011545962.2:c.*31_*44del XP_011544264.1:n.*31_*44del
XM_017023732.1:c.*31_*44del XP_016879221.1:n.*31_*44del
NM_025193.4:c.785_798del MANE Select NP_079469.2:p.Gly262GlufsTer?
NM_001142777.2:c.*31_*44del NP_001136249.1:n.*31_*44del
NM_001142778.2:c.*31_*44del NP_001136250.1:n.*31_*44del