Canonical Allele Identifier: CA1242195961

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526259G= , CM000664.2:g.31526259G=	GRCh38
NC_000002.11:g.31751329G= , CM000664.1:g.31751329G=	GRCh37
NC_000002.10:g.31604833G=	NCBI36
NG_008365.1:g.59713C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.702C= MANE Select	ENSP00000477587.1:p.Phe234=
ENST00000622030.1:c.702C=	ENSP00000477587.1:p.Phe234=
NM_000348.3:c.702C=	NP_000339.2:p.Phe234=
XM_011533069.1:c.480C=	XP_011531371.1:p.Phe160=
XM_011533070.1:c.447C=	XP_011531372.1:p.Phe149=
XM_011533071.1:c.447C=	XP_011531373.1:p.Phe149=
XM_011533072.1:c.447C=	XP_011531374.1:p.Phe149=
XM_011533069.2:c.480C=	XP_011531371.1:p.Phe160=
XM_011533072.2:c.447C=	XP_011531374.1:p.Phe149=
NM_000348.4:c.702C= MANE Select	NP_000339.2:p.Phe234=