Canonical Allele Identifier: CA2576929359
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31526164_31526165del , CM000664.2:g.31526164_31526165del GRCh38
NC_000002.11:g.31751234_31751235del , CM000664.1:g.31751234_31751235del GRCh37
NC_000002.10:g.31604738_31604739del NCBI36
NG_008365.1:g.59809_59810del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.*33_*34del MANE Select ENSP00000477587.1:n.*33_*34del
ENST00000622030.1:c.*33_*34del ENSP00000477587.1:n.*33_*34del
NM_000348.3:c.*33_*34del NP_000339.2:n.*33_*34del
XM_011533069.1:c.*33_*34del XP_011531371.1:n.*33_*34del
XM_011533070.1:c.*33_*34del XP_011531372.1:n.*33_*34del
XM_011533071.1:c.*33_*34del XP_011531373.1:n.*33_*34del
XM_011533072.1:c.*33_*34del XP_011531374.1:n.*33_*34del
XM_011533069.2:c.*33_*34del XP_011531371.1:n.*33_*34del
XM_011533072.2:c.*33_*34del XP_011531374.1:n.*33_*34del
NM_000348.4:c.*33_*34del MANE Select NP_000339.2:n.*33_*34del