Canonical Allele Identifier: CA1242196086

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1665788106

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526564del , CM000664.2:g.31526564del	GRCh38
NC_000002.11:g.31751634del , CM000664.1:g.31751634del	GRCh37
NC_000002.10:g.31605138del	NCBI36
NG_008365.1:g.59412del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-298del MANE Select	ENSP00000477587.1:n.699-298del
ENST00000622030.1:c.699-298del	ENSP00000477587.1:n.699-298del
NM_000348.3:c.699-298del	NP_000339.2:n.699-298del
XM_011533069.1:c.477-298del	XP_011531371.1:n.477-298del
XM_011533070.1:c.444-298del	XP_011531372.1:n.444-298del
XM_011533071.1:c.444-298del	XP_011531373.1:n.444-298del
XM_011533072.1:c.444-298del	XP_011531374.1:n.444-298del
XM_011533069.2:c.477-298del	XP_011531371.1:n.477-298del
XM_011533072.2:c.444-298del	XP_011531374.1:n.444-298del
NM_000348.4:c.699-298del MANE Select	NP_000339.2:n.699-298del