Canonical Allele Identifier: CA1028958616
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1666067895

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31538433del , CM000664.2:g.31538433del GRCh38
NC_000002.11:g.31763503del , CM000664.1:g.31763503del GRCh37
NC_000002.10:g.31617007del NCBI36
NG_008365.1:g.47541del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.282-4665del MANE Select ENSP00000477587.1:n.282-4665del
ENST00000622030.1:c.282-4665del ENSP00000477587.1:n.282-4665del
NM_000348.3:c.282-4665del NP_000339.2:n.282-4665del
XM_011533068.1:c.282-4665del XP_011531370.1:n.282-4665del
XM_011533069.1:c.60-4665del XP_011531371.1:n.60-4665del
XM_011533070.1:c.27-4665del XP_011531372.1:n.27-4665del
XM_011533071.1:c.27-4665del XP_011531373.1:n.27-4665del
XM_011533072.1:c.27-4665del XP_011531374.1:n.27-4665del
XM_011533069.2:c.60-4665del XP_011531371.1:n.60-4665del
XM_011533072.2:c.27-4665del XP_011531374.1:n.27-4665del
NM_000348.4:c.282-4665del MANE Select NP_000339.2:n.282-4665del