Canonical Allele Identifier: CA1242197377
Gene: SRD5A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.31529334A= , CM000664.2:g.31529334A= GRCh38
NC_000002.11:g.31754404A= , CM000664.1:g.31754404A= GRCh37
NC_000002.10:g.31607908A= NCBI36
NG_008365.1:g.56638T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622030.2:c.671T= MANE Select ENSP00000477587.1:p.Leu224=
ENST00000622030.1:c.671T= ENSP00000477587.1:p.Leu224=
NM_000348.3:c.671T= NP_000339.2:p.Leu224=
XM_011533069.1:c.449T= XP_011531371.1:p.Leu150=
XM_011533070.1:c.416T= XP_011531372.1:p.Leu139=
XM_011533071.1:c.416T= XP_011531373.1:p.Leu139=
XM_011533072.1:c.416T= XP_011531374.1:p.Leu139=
XM_011533069.2:c.449T= XP_011531371.1:p.Leu150=
XM_011533072.2:c.416T= XP_011531374.1:p.Leu139=
NM_000348.4:c.671T= MANE Select NP_000339.2:p.Leu224=