Canonical Allele Identifier: CA1242201359

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1666067813

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31538424_31538427del , CM000664.2:g.31538424_31538427del	GRCh38
NC_000002.11:g.31763494_31763497del , CM000664.1:g.31763494_31763497del	GRCh37
NC_000002.10:g.31616998_31617001del	NCBI36
NG_008365.1:g.47545_47548del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.282-4661_282-4658del MANE Select	ENSP00000477587.1:n.282-4661_282-4658del
ENST00000622030.1:c.282-4661_282-4658del	ENSP00000477587.1:n.282-4661_282-4658del
NM_000348.3:c.282-4661_282-4658del	NP_000339.2:n.282-4661_282-4658del
XM_011533068.1:c.282-4661_282-4658del	XP_011531370.1:n.282-4661_282-4658del
XM_011533069.1:c.60-4661_60-4658del	XP_011531371.1:n.60-4661_60-4658del
XM_011533070.1:c.27-4661_27-4658del	XP_011531372.1:n.27-4661_27-4658del
XM_011533071.1:c.27-4661_27-4658del	XP_011531373.1:n.27-4661_27-4658del
XM_011533072.1:c.27-4661_27-4658del	XP_011531374.1:n.27-4661_27-4658del
XM_011533069.2:c.60-4661_60-4658del	XP_011531371.1:n.60-4661_60-4658del
XM_011533072.2:c.27-4661_27-4658del	XP_011531374.1:n.27-4661_27-4658del
NM_000348.4:c.282-4661_282-4658del MANE Select	NP_000339.2:n.282-4661_282-4658del