Canonical Allele Identifier: CA1242195978
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31526287_31526291delinsGTAAA , CM000664.2:g.31526287_31526291delinsGTAAA GRCh38
NC_000002.11:g.31751357_31751361delinsGTAAA , CM000664.1:g.31751357_31751361delinsGTAAA GRCh37
NC_000002.10:g.31604861_31604865delinsGTAAA NCBI36
NG_008365.1:g.59681_59685delinsTTTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.699-29_699-25delinsTTTAC MANE Select ENSP00000477587.1:n.699-29_699-25delinsTTTAC
ENST00000622030.1:c.699-29_699-25delinsTTTAC ENSP00000477587.1:n.699-29_699-25delinsTTTAC
NM_000348.3:c.699-29_699-25delinsTTTAC NP_000339.2:n.699-29_699-25delinsTTTAC
XM_011533069.1:c.477-29_477-25delinsTTTAC XP_011531371.1:n.477-29_477-25delinsTTTAC
XM_011533070.1:c.444-29_444-25delinsTTTAC XP_011531372.1:n.444-29_444-25delinsTTTAC
XM_011533071.1:c.444-29_444-25delinsTTTAC XP_011531373.1:n.444-29_444-25delinsTTTAC
XM_011533072.1:c.444-29_444-25delinsTTTAC XP_011531374.1:n.444-29_444-25delinsTTTAC
XM_011533069.2:c.477-29_477-25delinsTTTAC XP_011531371.1:n.477-29_477-25delinsTTTAC
XM_011533072.2:c.444-29_444-25delinsTTTAC XP_011531374.1:n.444-29_444-25delinsTTTAC
NM_000348.4:c.699-29_699-25delinsTTTAC MANE Select NP_000339.2:n.699-29_699-25delinsTTTAC