Canonical Allele Identifier: CA1242196094

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1665788774

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526581del , CM000664.2:g.31526581del	GRCh38
NC_000002.11:g.31751651del , CM000664.1:g.31751651del	GRCh37
NC_000002.10:g.31605155del	NCBI36
NG_008365.1:g.59392del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-318del MANE Select	ENSP00000477587.1:n.699-318del
ENST00000622030.1:c.699-318del	ENSP00000477587.1:n.699-318del
NM_000348.3:c.699-318del	NP_000339.2:n.699-318del
XM_011533069.1:c.477-318del	XP_011531371.1:n.477-318del
XM_011533070.1:c.444-318del	XP_011531372.1:n.444-318del
XM_011533071.1:c.444-318del	XP_011531373.1:n.444-318del
XM_011533072.1:c.444-318del	XP_011531374.1:n.444-318del
XM_011533069.2:c.477-318del	XP_011531371.1:n.477-318del
XM_011533072.2:c.444-318del	XP_011531374.1:n.444-318del
NM_000348.4:c.699-318del MANE Select	NP_000339.2:n.699-318del