Canonical Allele Identifier: CA1028957277
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1665971633

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533954del , CM000664.2:g.31533954del GRCh38
NC_000002.11:g.31759024del , CM000664.1:g.31759024del GRCh37
NC_000002.10:g.31612528del NCBI36
NG_008365.1:g.52021del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.282-185del MANE Select ENSP00000477587.1:n.282-185del
ENST00000622030.1:c.282-185del ENSP00000477587.1:n.282-185del
NM_000348.3:c.282-185del NP_000339.2:n.282-185del
XM_011533068.1:c.282-185del XP_011531370.1:n.282-185del
XM_011533069.1:c.60-185del XP_011531371.1:n.60-185del
XM_011533070.1:c.27-185del XP_011531372.1:n.27-185del
XM_011533071.1:c.27-185del XP_011531373.1:n.27-185del
XM_011533072.1:c.27-185del XP_011531374.1:n.27-185del
XM_011533069.2:c.60-185del XP_011531371.1:n.60-185del
XM_011533072.2:c.27-185del XP_011531374.1:n.27-185del
NM_000348.4:c.282-185del MANE Select NP_000339.2:n.282-185del