Canonical Allele Identifier: CA2843338685
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31567454delinsATATA , CM000664.2:g.31567454delinsATATA GRCh38
NC_000002.11:g.31792524delinsATATA , CM000664.1:g.31792524delinsATATA GRCh37
NC_000002.10:g.31646028delinsATATA NCBI36
NG_008365.1:g.18518delinsTATAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+13166delinsTATAT MANE Select ENSP00000477587.1:n.281+13166delinsTATAT
ENST00000622030.1:c.281+13166delinsTATAT ENSP00000477587.1:n.281+13166delinsTATAT
NM_000348.3:c.281+13166delinsTATAT NP_000339.2:n.281+13166delinsTATAT
XM_011533068.1:c.281+13166delinsTATAT XP_011531370.1:n.281+13166delinsTATAT
XM_011533070.1:c.27-33688delinsTATAT XP_011531372.1:n.27-33688delinsTATAT
XM_011533071.1:c.27-33688delinsTATAT XP_011531373.1:n.27-33688delinsTATAT
XM_011533072.1:c.27-33688delinsTATAT XP_011531374.1:n.27-33688delinsTATAT
XM_011533072.2:c.27-33688delinsTATAT XP_011531374.1:n.27-33688delinsTATAT
NM_000348.4:c.281+13166delinsTATAT MANE Select NP_000339.2:n.281+13166delinsTATAT