Canonical Allele Identifier: CA1028962852
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1665859435

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529505del , CM000664.2:g.31529505del GRCh38
NC_000002.11:g.31754575del , CM000664.1:g.31754575del GRCh37
NC_000002.10:g.31608079del NCBI36
NG_008365.1:g.56470del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.548-45del MANE Select ENSP00000477587.1:n.548-45del
ENST00000622030.1:c.548-45del ENSP00000477587.1:n.548-45del
NM_000348.3:c.548-45del NP_000339.2:n.548-45del
XM_011533069.1:c.326-45del XP_011531371.1:n.326-45del
XM_011533070.1:c.293-45del XP_011531372.1:n.293-45del
XM_011533071.1:c.293-45del XP_011531373.1:n.293-45del
XM_011533072.1:c.293-45del XP_011531374.1:n.293-45del
XM_011533069.2:c.326-45del XP_011531371.1:n.326-45del
XM_011533072.2:c.293-45del XP_011531374.1:n.293-45del
NM_000348.4:c.548-45del MANE Select NP_000339.2:n.548-45del