Canonical Allele Identifier: CA2698936859

Gene: SRD5A2

Linked Data

• dbSNP Id: rs2148066755

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533571del , CM000664.2:g.31533571del	GRCh38
NC_000002.11:g.31758641del , CM000664.1:g.31758641del	GRCh37
NC_000002.10:g.31612145del	NCBI36
NG_008365.1:g.52403del

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.445+34del MANE Select	ENSP00000477587.1:n.445+34del
ENST00000622030.1:c.445+34del	ENSP00000477587.1:n.445+34del
NM_000348.3:c.445+34del	NP_000339.2:n.445+34del
XM_011533068.1:c.445+34del	XP_011531370.1:n.445+34del
XM_011533069.1:c.223+34del	XP_011531371.1:n.223+34del
XM_011533070.1:c.190+34del	XP_011531372.1:n.190+34del
XM_011533071.1:c.190+34del	XP_011531373.1:n.190+34del
XM_011533072.1:c.190+34del	XP_011531374.1:n.190+34del
XM_011533069.2:c.223+34del	XP_011531371.1:n.223+34del
XM_011533072.2:c.190+34del	XP_011531374.1:n.190+34del
NM_000348.4:c.445+34del MANE Select	NP_000339.2:n.445+34del