Canonical Allele Identifier: CA1242197314

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529218C= , CM000664.2:g.31529218C=	GRCh38
NC_000002.11:g.31754288C= , CM000664.1:g.31754288C=	GRCh37
NC_000002.10:g.31607792C=	NCBI36
NG_008365.1:g.56754G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.698+89G= MANE Select	ENSP00000477587.1:n.698+89G=
ENST00000622030.1:c.698+89G=	ENSP00000477587.1:n.698+89G=
NM_000348.3:c.698+89G=	NP_000339.2:n.698+89G=
XM_011533069.1:c.476+89G=	XP_011531371.1:n.476+89G=
XM_011533070.1:c.443+89G=	XP_011531372.1:n.443+89G=
XM_011533071.1:c.443+89G=	XP_011531373.1:n.443+89G=
XM_011533072.1:c.443+89G=	XP_011531374.1:n.443+89G=
XM_011533069.2:c.476+89G=	XP_011531371.1:n.476+89G=
XM_011533072.2:c.443+89G=	XP_011531374.1:n.443+89G=
NM_000348.4:c.698+89G= MANE Select	NP_000339.2:n.698+89G=