Canonical Allele Identifier: CA1242195996

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526331C= , CM000664.2:g.31526331C=	GRCh38
NC_000002.11:g.31751401C= , CM000664.1:g.31751401C=	GRCh37
NC_000002.10:g.31604905C=	NCBI36
NG_008365.1:g.59641G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-69G= MANE Select	ENSP00000477587.1:n.699-69G=
ENST00000622030.1:c.699-69G=	ENSP00000477587.1:n.699-69G=
NM_000348.3:c.699-69G=	NP_000339.2:n.699-69G=
XM_011533069.1:c.477-69G=	XP_011531371.1:n.477-69G=
XM_011533070.1:c.444-69G=	XP_011531372.1:n.444-69G=
XM_011533071.1:c.444-69G=	XP_011531373.1:n.444-69G=
XM_011533072.1:c.444-69G=	XP_011531374.1:n.444-69G=
XM_011533069.2:c.477-69G=	XP_011531371.1:n.477-69G=
XM_011533072.2:c.444-69G=	XP_011531374.1:n.444-69G=
NM_000348.4:c.699-69G= MANE Select	NP_000339.2:n.699-69G=