Canonical Allele Identifier: CA1242197428
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529443_31529444delinsAC , CM000664.2:g.31529443_31529444delinsAC GRCh38
NC_000002.11:g.31754513_31754514delinsAC , CM000664.1:g.31754513_31754514delinsAC GRCh37
NC_000002.10:g.31608017_31608018delinsAC NCBI36
NG_008365.1:g.56528_56529delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.561_562delinsGT MANE Select ENSP00000477587.1:p.Thr187=
ENST00000622030.1:c.561_562delinsGT ENSP00000477587.1:p.Thr187=
NM_000348.3:c.561_562delinsGT NP_000339.2:p.Thr187=
XM_011533069.1:c.339_340delinsGT XP_011531371.1:p.Thr113=
XM_011533070.1:c.306_307delinsGT XP_011531372.1:p.Thr102=
XM_011533071.1:c.306_307delinsGT XP_011531373.1:p.Thr102=
XM_011533072.1:c.306_307delinsGT XP_011531374.1:p.Thr102=
XM_011533069.2:c.339_340delinsGT XP_011531371.1:p.Thr113=
XM_011533072.2:c.306_307delinsGT XP_011531374.1:p.Thr102=
NM_000348.4:c.561_562delinsGT MANE Select NP_000339.2:p.Thr187=