Canonical Allele Identifier: CA1242214634
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31567456_31567458delinsGTA , CM000664.2:g.31567456_31567458delinsGTA GRCh38
NC_000002.11:g.31792526_31792528delinsGTA , CM000664.1:g.31792526_31792528delinsGTA GRCh37
NC_000002.10:g.31646030_31646032delinsGTA NCBI36
NG_008365.1:g.18514_18516delinsTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+13162_281+13164delinsTAC MANE Select ENSP00000477587.1:n.281+13162_281+13164delinsTAC
ENST00000622030.1:c.281+13162_281+13164delinsTAC ENSP00000477587.1:n.281+13162_281+13164delinsTAC
NM_000348.3:c.281+13162_281+13164delinsTAC NP_000339.2:n.281+13162_281+13164delinsTAC
XM_011533068.1:c.281+13162_281+13164delinsTAC XP_011531370.1:n.281+13162_281+13164delinsTAC
XM_011533070.1:c.27-33692_27-33690delinsTAC XP_011531372.1:n.27-33692_27-33690delinsTAC
XM_011533071.1:c.27-33692_27-33690delinsTAC XP_011531373.1:n.27-33692_27-33690delinsTAC
XM_011533072.1:c.27-33692_27-33690delinsTAC XP_011531374.1:n.27-33692_27-33690delinsTAC
XM_011533072.2:c.27-33692_27-33690delinsTAC XP_011531374.1:n.27-33692_27-33690delinsTAC
NM_000348.4:c.281+13162_281+13164delinsTAC MANE Select NP_000339.2:n.281+13162_281+13164delinsTAC