Canonical Allele Identifier: CA2658498438
Gene: SRD5A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31531265del , CM000664.2:g.31531265del GRCh38
NC_000002.11:g.31756335del , CM000664.1:g.31756335del GRCh37
NC_000002.10:g.31609839del NCBI36
NG_008365.1:g.54708del

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.547+107del MANE Select ENSP00000477587.1:n.547+107del
ENST00000622030.1:c.547+107del ENSP00000477587.1:n.547+107del
NM_000348.3:c.547+107del NP_000339.2:n.547+107del
XM_011533069.1:c.325+107del XP_011531371.1:n.325+107del
XM_011533070.1:c.292+107del XP_011531372.1:n.292+107del
XM_011533071.1:c.292+107del XP_011531373.1:n.292+107del
XM_011533072.1:c.292+107del XP_011531374.1:n.292+107del
XM_011533069.2:c.325+107del XP_011531371.1:n.325+107del
XM_011533072.2:c.292+107del XP_011531374.1:n.292+107del
NM_000348.4:c.547+107del MANE Select NP_000339.2:n.547+107del