Canonical Allele Identifier: CA1242199258

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533506T= , CM000664.2:g.31533506T=	GRCh38
NC_000002.11:g.31758576T= , CM000664.1:g.31758576T=	GRCh37
NC_000002.10:g.31612080T=	NCBI36
NG_008365.1:g.52466A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.445+97A= MANE Select	ENSP00000477587.1:n.445+97A=
ENST00000622030.1:c.445+97A=	ENSP00000477587.1:n.445+97A=
NM_000348.3:c.445+97A=	NP_000339.2:n.445+97A=
XM_011533068.1:c.445+97A=	XP_011531370.1:n.445+97A=
XM_011533069.1:c.223+97A=	XP_011531371.1:n.223+97A=
XM_011533070.1:c.190+97A=	XP_011531372.1:n.190+97A=
XM_011533071.1:c.190+97A=	XP_011531373.1:n.190+97A=
XM_011533072.1:c.190+97A=	XP_011531374.1:n.190+97A=
XM_011533069.2:c.223+97A=	XP_011531371.1:n.223+97A=
XM_011533072.2:c.190+97A=	XP_011531374.1:n.190+97A=
NM_000348.4:c.445+97A= MANE Select	NP_000339.2:n.445+97A=