Canonical Allele Identifier: CA115825
Gene: HSD3B7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2882
dbSNP Id: rs397514443

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30986176dup , CM000678.2:g.30986176dup GRCh38
NC_000016.9:g.30997497dup , CM000678.1:g.30997497dup GRCh37
NC_000016.8:g.30904998dup NCBI36
NG_012346.1:g.5979dup
NG_052948.1:g.33883dup

Transcript Alleles

HGVS Amino-acid change
ENST00000297679.10:c.294dup MANE Select ENSP00000297679.5:p.Lys99GlnfsTer5
ENST00000262520.10:c.294dup ENSP00000262520.6:p.Lys99GlnfsTer5
ENST00000297679.9:c.294dup ENSP00000297679.5:p.Lys99GlnfsTer5
ENST00000562932.5:c.417dup ENSP00000459852.1:p.Lys140GlnfsTer5
ENST00000574447.1:c.294dup ENSP00000459689.1:p.Lys99GlnfsTer5
NM_001142777.1:c.294dup NP_001136249.1:p.Lys99GlnfsTer5
NM_001142778.1:c.294dup NP_001136250.1:p.Lys99GlnfsTer5
NM_025193.3:c.294dup NP_079469.2:p.Lys99GlnfsTer5
XM_005255601.3:c.294dup XP_005255658.2:p.Lys99GlnfsTer5
XM_011545960.1:c.294dup XP_011544262.1:p.Lys99GlnfsTer5
XM_011545961.1:c.294dup XP_011544263.1:p.Lys99GlnfsTer5
XM_011545962.1:c.294dup XP_011544264.1:p.Lys99GlnfsTer5
XM_011545960.2:c.294dup XP_011544262.1:p.Lys99GlnfsTer5
XM_011545962.2:c.294dup XP_011544264.1:p.Lys99GlnfsTer5
XM_017023732.1:c.294dup XP_016879221.1:p.Lys99GlnfsTer5
NM_025193.4:c.294dup MANE Select NP_079469.2:p.Lys99GlnfsTer5
NM_001142777.2:c.294dup NP_001136249.1:p.Lys99GlnfsTer5
NM_001142778.2:c.294dup NP_001136250.1:p.Lys99GlnfsTer5