Canonical Allele Identifier: CA1242199386

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31533778_31533779delinsAG , CM000664.2:g.31533778_31533779delinsAG	GRCh38
NC_000002.11:g.31758848_31758849delinsAG , CM000664.1:g.31758848_31758849delinsAG	GRCh37
NC_000002.10:g.31612352_31612353delinsAG	NCBI36
NG_008365.1:g.52193_52194delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.282-13_282-12delinsCT MANE Select	ENSP00000477587.1:n.282-13_282-12delinsCT
ENST00000622030.1:c.282-13_282-12delinsCT	ENSP00000477587.1:n.282-13_282-12delinsCT
NM_000348.3:c.282-13_282-12delinsCT	NP_000339.2:n.282-13_282-12delinsCT
XM_011533068.1:c.282-13_282-12delinsCT	XP_011531370.1:n.282-13_282-12delinsCT
XM_011533069.1:c.60-13_60-12delinsCT	XP_011531371.1:n.60-13_60-12delinsCT
XM_011533070.1:c.27-13_27-12delinsCT	XP_011531372.1:n.27-13_27-12delinsCT
XM_011533071.1:c.27-13_27-12delinsCT	XP_011531373.1:n.27-13_27-12delinsCT
XM_011533072.1:c.27-13_27-12delinsCT	XP_011531374.1:n.27-13_27-12delinsCT
XM_011533069.2:c.60-13_60-12delinsCT	XP_011531371.1:n.60-13_60-12delinsCT
XM_011533072.2:c.27-13_27-12delinsCT	XP_011531374.1:n.27-13_27-12delinsCT
NM_000348.4:c.282-13_282-12delinsCT MANE Select	NP_000339.2:n.282-13_282-12delinsCT