Canonical Allele Identifier: CA2658499349

Gene: SRD5A2

Linked Data

• gnomAD v4: 2-31533829-ACCTCTTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533831_31533837del , CM000664.2:g.31533831_31533837del	GRCh38
NC_000002.11:g.31758901_31758907del , CM000664.1:g.31758901_31758907del	GRCh37
NC_000002.10:g.31612405_31612411del	NCBI36
NG_008365.1:g.52136_52142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.282-70_282-64del MANE Select	ENSP00000477587.1:n.282-70_282-64del
ENST00000622030.1:c.282-70_282-64del	ENSP00000477587.1:n.282-70_282-64del
NM_000348.3:c.282-70_282-64del	NP_000339.2:n.282-70_282-64del
XM_011533068.1:c.282-70_282-64del	XP_011531370.1:n.282-70_282-64del
XM_011533069.1:c.60-70_60-64del	XP_011531371.1:n.60-70_60-64del
XM_011533070.1:c.27-70_27-64del	XP_011531372.1:n.27-70_27-64del
XM_011533071.1:c.27-70_27-64del	XP_011531373.1:n.27-70_27-64del
XM_011533072.1:c.27-70_27-64del	XP_011531374.1:n.27-70_27-64del
XM_011533069.2:c.60-70_60-64del	XP_011531371.1:n.60-70_60-64del
XM_011533072.2:c.27-70_27-64del	XP_011531374.1:n.27-70_27-64del
NM_000348.4:c.282-70_282-64del MANE Select	NP_000339.2:n.282-70_282-64del