Canonical Allele Identifier: CA1242197457
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529501_31529502delinsAT , CM000664.2:g.31529501_31529502delinsAT GRCh38
NC_000002.11:g.31754571_31754572delinsAT , CM000664.1:g.31754571_31754572delinsAT GRCh37
NC_000002.10:g.31608075_31608076delinsAT NCBI36
NG_008365.1:g.56470_56471delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.548-45_548-44delinsAT MANE Select ENSP00000477587.1:n.548-45_548-44delinsAT
ENST00000622030.1:c.548-45_548-44delinsAT ENSP00000477587.1:n.548-45_548-44delinsAT
NM_000348.3:c.548-45_548-44delinsAT NP_000339.2:n.548-45_548-44delinsAT
XM_011533069.1:c.326-45_326-44delinsAT XP_011531371.1:n.326-45_326-44delinsAT
XM_011533070.1:c.293-45_293-44delinsAT XP_011531372.1:n.293-45_293-44delinsAT
XM_011533071.1:c.293-45_293-44delinsAT XP_011531373.1:n.293-45_293-44delinsAT
XM_011533072.1:c.293-45_293-44delinsAT XP_011531374.1:n.293-45_293-44delinsAT
XM_011533069.2:c.326-45_326-44delinsAT XP_011531371.1:n.326-45_326-44delinsAT
XM_011533072.2:c.293-45_293-44delinsAT XP_011531374.1:n.293-45_293-44delinsAT
NM_000348.4:c.548-45_548-44delinsAT MANE Select NP_000339.2:n.548-45_548-44delinsAT