Canonical Allele Identifier: CA1242214632

Gene: SRD5A2

Linked Data

• dbSNP Id: rs575917234

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567455_31567456insATGTAT , CM000664.2:g.31567455_31567456insATGTAT	GRCh38
NC_000002.11:g.31792525_31792526insATGTAT , CM000664.1:g.31792525_31792526insATGTAT	GRCh37
NC_000002.10:g.31646029_31646030insATGTAT	NCBI36
NG_008365.1:g.18517_18518insTACATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13165_281+13166insTACATA MANE Select	ENSP00000477587.1:n.281+13165_281+13166insTACATA
ENST00000622030.1:c.281+13165_281+13166insTACATA	ENSP00000477587.1:n.281+13165_281+13166insTACATA
NM_000348.3:c.281+13165_281+13166insTACATA	NP_000339.2:n.281+13165_281+13166insTACATA
XM_011533068.1:c.281+13165_281+13166insTACATA	XP_011531370.1:n.281+13165_281+13166insTACATA
XM_011533070.1:c.27-33689_27-33688insTACATA	XP_011531372.1:n.27-33689_27-33688insTACATA
XM_011533071.1:c.27-33689_27-33688insTACATA	XP_011531373.1:n.27-33689_27-33688insTACATA
XM_011533072.1:c.27-33689_27-33688insTACATA	XP_011531374.1:n.27-33689_27-33688insTACATA
XM_011533072.2:c.27-33689_27-33688insTACATA	XP_011531374.1:n.27-33689_27-33688insTACATA
NM_000348.4:c.281+13165_281+13166insTACATA MANE Select	NP_000339.2:n.281+13165_281+13166insTACATA