Canonical Allele Identifier: CA2658499468
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31533917dup , CM000664.2:g.31533917dup GRCh38
NC_000002.11:g.31758987dup , CM000664.1:g.31758987dup GRCh37
NC_000002.10:g.31612491dup NCBI36
NG_008365.1:g.52055dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.282-151dup MANE Select ENSP00000477587.1:n.282-151dup
ENST00000622030.1:c.282-151dup ENSP00000477587.1:n.282-151dup
NM_000348.3:c.282-151dup NP_000339.2:n.282-151dup
XM_011533068.1:c.282-151dup XP_011531370.1:n.282-151dup
XM_011533069.1:c.60-151dup XP_011531371.1:n.60-151dup
XM_011533070.1:c.27-151dup XP_011531372.1:n.27-151dup
XM_011533071.1:c.27-151dup XP_011531373.1:n.27-151dup
XM_011533072.1:c.27-151dup XP_011531374.1:n.27-151dup
XM_011533069.2:c.60-151dup XP_011531371.1:n.60-151dup
XM_011533072.2:c.27-151dup XP_011531374.1:n.27-151dup
NM_000348.4:c.282-151dup MANE Select NP_000339.2:n.282-151dup