Canonical Allele Identifier: CA916503719

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1558372186

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567456_31567461dup , CM000664.2:g.31567456_31567461dup	GRCh38
NC_000002.11:g.31792526_31792531dup , CM000664.1:g.31792526_31792531dup	GRCh37
NC_000002.10:g.31646030_31646035dup	NCBI36
NG_008365.1:g.18512_18517dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13160_281+13165dup MANE Select	ENSP00000477587.1:n.281+13160_281+13165dup
ENST00000622030.1:c.281+13160_281+13165dup	ENSP00000477587.1:n.281+13160_281+13165dup
NM_000348.3:c.281+13160_281+13165dup	NP_000339.2:n.281+13160_281+13165dup
XM_011533068.1:c.281+13160_281+13165dup	XP_011531370.1:n.281+13160_281+13165dup
XM_011533070.1:c.27-33694_27-33689dup	XP_011531372.1:n.27-33694_27-33689dup
XM_011533071.1:c.27-33694_27-33689dup	XP_011531373.1:n.27-33694_27-33689dup
XM_011533072.1:c.27-33694_27-33689dup	XP_011531374.1:n.27-33694_27-33689dup
XM_011533072.2:c.27-33694_27-33689dup	XP_011531374.1:n.27-33694_27-33689dup
NM_000348.4:c.281+13160_281+13165dup MANE Select	NP_000339.2:n.281+13160_281+13165dup