Canonical Allele Identifier: CA1192292485
Gene: HSD3B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119422005_119422014delinsTAATGGGTGG , CM000663.2:g.119422005_119422014delinsTAATGGGTGG GRCh38
NC_000001.10:g.119964628_119964637delinsTAATGGGTGG , CM000663.1:g.119964628_119964637delinsTAATGGGTGG GRCh37
NC_000001.9:g.119766151_119766160delinsTAATGGGTGG NCBI36
NG_013349.1:g.12075_12084delinsTAATGGGTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369416.4:c.504_513delinsTAATGGGTGG MANE Select ENSP00000358424.3:p.Ala168=
ENST00000369416.3:c.504_513delinsTAATGGGTGG ENSP00000358424.3:p.Ala168=
ENST00000433745.5:c.504_513delinsTAATGGGTGG ENSP00000388292.1:p.Ala168=
ENST00000448448.2:n.448_457delinsTAATGGGTGG
ENST00000543831.5:c.504_513delinsTAATGGGTGG ENSP00000445122.1:p.Ala168=
NM_000198.3:c.504_513delinsTAATGGGTGG NP_000189.1:p.Ala168=
NM_001166120.1:c.504_513delinsTAATGGGTGG NP_001159592.1:p.Ala168=
NM_000198.4:c.504_513delinsTAATGGGTGG MANE Select NP_000189.1:p.Ala168=
NM_001166120.2:c.504_513delinsTAATGGGTGG NP_001159592.1:p.Ala168=