Canonical Allele Identifier: CA2502191688
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31526592del , CM000664.2:g.31526592del GRCh38
NC_000002.11:g.31751662del , CM000664.1:g.31751662del GRCh37
NC_000002.10:g.31605166del NCBI36
NG_008365.1:g.59388del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.699-322del MANE Select ENSP00000477587.1:n.699-322del
ENST00000622030.1:c.699-322del ENSP00000477587.1:n.699-322del
NM_000348.3:c.699-322del NP_000339.2:n.699-322del
XM_011533069.1:c.477-322del XP_011531371.1:n.477-322del
XM_011533070.1:c.444-322del XP_011531372.1:n.444-322del
XM_011533071.1:c.444-322del XP_011531373.1:n.444-322del
XM_011533072.1:c.444-322del XP_011531374.1:n.444-322del
XM_011533069.2:c.477-322del XP_011531371.1:n.477-322del
XM_011533072.2:c.444-322del XP_011531374.1:n.444-322del
NM_000348.4:c.699-322del MANE Select NP_000339.2:n.699-322del