Canonical Allele Identifier: CA531712329
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1216933026

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531377del , CM000664.2:g.31531377del GRCh38
NC_000002.11:g.31756447del , CM000664.1:g.31756447del GRCh37
NC_000002.10:g.31609951del NCBI36
NG_008365.1:g.54596del

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.542del MANE Select ENSP00000477587.1:p.Pro181HisfsTer?
ENST00000622030.1:c.542del ENSP00000477587.1:p.Pro181HisfsTer?
NM_000348.3:c.542del NP_000339.2:p.Pro181HisfsTer?
XM_011533069.1:c.320del XP_011531371.1:p.Pro107HisfsTer?
XM_011533070.1:c.287del XP_011531372.1:p.Pro96HisfsTer?
XM_011533071.1:c.287del XP_011531373.1:p.Pro96HisfsTer?
XM_011533072.1:c.287del XP_011531374.1:p.Pro96HisfsTer?
XM_011533069.2:c.320del XP_011531371.1:p.Pro107HisfsTer?
XM_011533072.2:c.287del XP_011531374.1:p.Pro96HisfsTer?
NM_000348.4:c.542del MANE Select NP_000339.2:p.Pro181HisfsTer?