Canonical Allele Identifier: CA2507014568

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567451_31567452insATAT , CM000664.2:g.31567451_31567452insATAT	GRCh38
NC_000002.11:g.31792521_31792522insATAT , CM000664.1:g.31792521_31792522insATAT	GRCh37
NC_000002.10:g.31646025_31646026insATAT	NCBI36
NG_008365.1:g.18521_18522insTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13169_281+13170insTATA MANE Select	ENSP00000477587.1:n.281+13169_281+13170insTATA
ENST00000622030.1:c.281+13169_281+13170insTATA	ENSP00000477587.1:n.281+13169_281+13170insTATA
NM_000348.3:c.281+13169_281+13170insTATA	NP_000339.2:n.281+13169_281+13170insTATA
XM_011533068.1:c.281+13169_281+13170insTATA	XP_011531370.1:n.281+13169_281+13170insTATA
XM_011533070.1:c.27-33685_27-33684insTATA	XP_011531372.1:n.27-33685_27-33684insTATA
XM_011533071.1:c.27-33685_27-33684insTATA	XP_011531373.1:n.27-33685_27-33684insTATA
XM_011533072.1:c.27-33685_27-33684insTATA	XP_011531374.1:n.27-33685_27-33684insTATA
XM_011533072.2:c.27-33685_27-33684insTATA	XP_011531374.1:n.27-33685_27-33684insTATA
NM_000348.4:c.281+13169_281+13170insTATA MANE Select	NP_000339.2:n.281+13169_281+13170insTATA