Canonical Allele Identifier: CA2698936272

Gene: SRD5A2

Linked Data

• dbSNP Id: rs2148094575

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567470_31567471insCATATA , CM000664.2:g.31567470_31567471insCATATA	GRCh38
NC_000002.11:g.31792540_31792541insCATATA , CM000664.1:g.31792540_31792541insCATATA	GRCh37
NC_000002.10:g.31646044_31646045insCATATA	NCBI36
NG_008365.1:g.18506_18507insGTATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13154_281+13155insGTATAT MANE Select	ENSP00000477587.1:n.281+13154_281+13155insGTATAT
ENST00000622030.1:c.281+13154_281+13155insGTATAT	ENSP00000477587.1:n.281+13154_281+13155insGTATAT
NM_000348.3:c.281+13154_281+13155insGTATAT	NP_000339.2:n.281+13154_281+13155insGTATAT
XM_011533068.1:c.281+13154_281+13155insGTATAT	XP_011531370.1:n.281+13154_281+13155insGTATAT
XM_011533070.1:c.27-33700_27-33699insGTATAT	XP_011531372.1:n.27-33700_27-33699insGTATAT
XM_011533071.1:c.27-33700_27-33699insGTATAT	XP_011531373.1:n.27-33700_27-33699insGTATAT
XM_011533072.1:c.27-33700_27-33699insGTATAT	XP_011531374.1:n.27-33700_27-33699insGTATAT
XM_011533072.2:c.27-33700_27-33699insGTATAT	XP_011531374.1:n.27-33700_27-33699insGTATAT
NM_000348.4:c.281+13154_281+13155insGTATAT MANE Select	NP_000339.2:n.281+13154_281+13155insGTATAT