Canonical Allele Identifier: CA1242199338
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533682_31533683delinsAT , CM000664.2:g.31533682_31533683delinsAT GRCh38
NC_000002.11:g.31758752_31758753delinsAT , CM000664.1:g.31758752_31758753delinsAT GRCh37
NC_000002.10:g.31612256_31612257delinsAT NCBI36
NG_008365.1:g.52289_52290delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000622030.2:c.365_366delinsAT MANE Select ENSP00000477587.1:p.Asn122=
ENST00000622030.1:c.365_366delinsAT ENSP00000477587.1:p.Asn122=
NM_000348.3:c.365_366delinsAT NP_000339.2:p.Asn122=
XM_011533068.1:c.365_366delinsAT XP_011531370.1:p.Asn122=
XM_011533069.1:c.143_144delinsAT XP_011531371.1:p.Asn48=
XM_011533070.1:c.110_111delinsAT XP_011531372.1:p.Asn37=
XM_011533071.1:c.110_111delinsAT XP_011531373.1:p.Asn37=
XM_011533072.1:c.110_111delinsAT XP_011531374.1:p.Asn37=
XM_011533069.2:c.143_144delinsAT XP_011531371.1:p.Asn48=
XM_011533072.2:c.110_111delinsAT XP_011531374.1:p.Asn37=
NM_000348.4:c.365_366delinsAT MANE Select NP_000339.2:p.Asn122=