Canonical Allele Identifier: CA2749374950
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31526183dup , CM000664.2:g.31526183dup GRCh38
NC_000002.11:g.31751253dup , CM000664.1:g.31751253dup GRCh37
NC_000002.10:g.31604757dup NCBI36
NG_008365.1:g.59793dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.*17dup MANE Select ENSP00000477587.1:n.*17dup
ENST00000622030.1:c.*17dup ENSP00000477587.1:n.*17dup
NM_000348.3:c.*17dup NP_000339.2:n.*17dup
XM_011533069.1:c.*17dup XP_011531371.1:n.*17dup
XM_011533070.1:c.*17dup XP_011531372.1:n.*17dup
XM_011533071.1:c.*17dup XP_011531373.1:n.*17dup
XM_011533072.1:c.*17dup XP_011531374.1:n.*17dup
XM_011533069.2:c.*17dup XP_011531371.1:n.*17dup
XM_011533072.2:c.*17dup XP_011531374.1:n.*17dup
NM_000348.4:c.*17dup MANE Select NP_000339.2:n.*17dup