Canonical Allele Identifier: CA1242197417
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529417_31529418delinsAC , CM000664.2:g.31529417_31529418delinsAC GRCh38
NC_000002.11:g.31754487_31754488delinsAC , CM000664.1:g.31754487_31754488delinsAC GRCh37
NC_000002.10:g.31607991_31607992delinsAC NCBI36
NG_008365.1:g.56554_56555delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.587_588delinsGT MANE Select ENSP00000477587.1:p.Gly196=
ENST00000622030.1:c.587_588delinsGT ENSP00000477587.1:p.Gly196=
NM_000348.3:c.587_588delinsGT NP_000339.2:p.Gly196=
XM_011533069.1:c.365_366delinsGT XP_011531371.1:p.Gly122=
XM_011533070.1:c.332_333delinsGT XP_011531372.1:p.Gly111=
XM_011533071.1:c.332_333delinsGT XP_011531373.1:p.Gly111=
XM_011533072.1:c.332_333delinsGT XP_011531374.1:p.Gly111=
XM_011533069.2:c.365_366delinsGT XP_011531371.1:p.Gly122=
XM_011533072.2:c.332_333delinsGT XP_011531374.1:p.Gly111=
NM_000348.4:c.587_588delinsGT MANE Select NP_000339.2:p.Gly196=