Canonical Allele Identifier: CA1242196083

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1665785757

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526559dup , CM000664.2:g.31526559dup	GRCh38
NC_000002.11:g.31751629dup , CM000664.1:g.31751629dup	GRCh37
NC_000002.10:g.31605133dup	NCBI36
NG_008365.1:g.59416dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-294dup MANE Select	ENSP00000477587.1:n.699-294dup
ENST00000622030.1:c.699-294dup	ENSP00000477587.1:n.699-294dup
NM_000348.3:c.699-294dup	NP_000339.2:n.699-294dup
XM_011533069.1:c.477-294dup	XP_011531371.1:n.477-294dup
XM_011533070.1:c.444-294dup	XP_011531372.1:n.444-294dup
XM_011533071.1:c.444-294dup	XP_011531373.1:n.444-294dup
XM_011533072.1:c.444-294dup	XP_011531374.1:n.444-294dup
XM_011533069.2:c.477-294dup	XP_011531371.1:n.477-294dup
XM_011533072.2:c.444-294dup	XP_011531374.1:n.444-294dup
NM_000348.4:c.699-294dup MANE Select	NP_000339.2:n.699-294dup