Canonical Allele Identifier: CA2658512682
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31580595_31580596insA , CM000664.2:g.31580595_31580596insA GRCh38
NC_000002.11:g.31805665_31805666insA , CM000664.1:g.31805665_31805666insA GRCh37
NC_000002.10:g.31659169_31659170insA NCBI36
NG_008365.1:g.5376_5377insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.281+24_281+25insT MANE Select ENSP00000477587.1:n.281+24_281+25insT
ENST00000622030.1:c.281+24_281+25insT ENSP00000477587.1:n.281+24_281+25insT
NM_000348.3:c.281+24_281+25insT NP_000339.2:n.281+24_281+25insT
XM_011533068.1:c.281+24_281+25insT XP_011531370.1:n.281+24_281+25insT
XM_011533070.1:c.27-46830_27-46829insT XP_011531372.1:n.27-46830_27-46829insT
XM_011533071.1:c.27-46830_27-46829insT XP_011531373.1:n.27-46830_27-46829insT
XM_011533072.1:c.27-46830_27-46829insT XP_011531374.1:n.27-46830_27-46829insT
XM_011533072.2:c.27-46830_27-46829insT XP_011531374.1:n.27-46830_27-46829insT
NM_000348.4:c.281+24_281+25insT MANE Select NP_000339.2:n.281+24_281+25insT