Canonical Allele Identifier: CA1242198316
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531400G= , CM000664.2:g.31531400G= GRCh38
NC_000002.11:g.31756470G= , CM000664.1:g.31756470G= GRCh37
NC_000002.10:g.31609974G= NCBI36
NG_008365.1:g.54572C=

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.518C= MANE Select ENSP00000477587.1:p.Pro173=
ENST00000622030.1:c.518C= ENSP00000477587.1:p.Pro173=
NM_000348.3:c.518C= NP_000339.2:p.Pro173=
XM_011533069.1:c.296C= XP_011531371.1:p.Pro99=
XM_011533070.1:c.263C= XP_011531372.1:p.Pro88=
XM_011533071.1:c.263C= XP_011531373.1:p.Pro88=
XM_011533072.1:c.263C= XP_011531374.1:p.Pro88=
XM_011533069.2:c.296C= XP_011531371.1:p.Pro99=
XM_011533072.2:c.263C= XP_011531374.1:p.Pro88=
NM_000348.4:c.518C= MANE Select NP_000339.2:p.Pro173=