Canonical Allele Identifier: CA1242214622
Gene: SRD5A2 HGNC NCBI

Linked Data

dbSNP Id: rs1261044976

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31567451_31567452insATATAT , CM000664.2:g.31567451_31567452insATATAT GRCh38
NC_000002.11:g.31792521_31792522insATATAT , CM000664.1:g.31792521_31792522insATATAT GRCh37
NC_000002.10:g.31646025_31646026insATATAT NCBI36
NG_008365.1:g.18521_18522insTATATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+13169_281+13170insTATATA MANE Select ENSP00000477587.1:n.281+13169_281+13170insTATATA
ENST00000622030.1:c.281+13169_281+13170insTATATA ENSP00000477587.1:n.281+13169_281+13170insTATATA
NM_000348.3:c.281+13169_281+13170insTATATA NP_000339.2:n.281+13169_281+13170insTATATA
XM_011533068.1:c.281+13169_281+13170insTATATA XP_011531370.1:n.281+13169_281+13170insTATATA
XM_011533070.1:c.27-33685_27-33684insTATATA XP_011531372.1:n.27-33685_27-33684insTATATA
XM_011533071.1:c.27-33685_27-33684insTATATA XP_011531373.1:n.27-33685_27-33684insTATATA
XM_011533072.1:c.27-33685_27-33684insTATATA XP_011531374.1:n.27-33685_27-33684insTATATA
XM_011533072.2:c.27-33685_27-33684insTATATA XP_011531374.1:n.27-33685_27-33684insTATATA
NM_000348.4:c.281+13169_281+13170insTATATA MANE Select NP_000339.2:n.281+13169_281+13170insTATATA