Canonical Allele Identifier: CA2568234628

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31538525_31538526insC , CM000664.2:g.31538525_31538526insC	GRCh38
NC_000002.11:g.31763595_31763596insC , CM000664.1:g.31763595_31763596insC	GRCh37
NC_000002.10:g.31617099_31617100insC	NCBI36
NG_008365.1:g.47446_47447insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.282-4760_282-4759insG MANE Select	ENSP00000477587.1:n.282-4760_282-4759insG
ENST00000622030.1:c.282-4760_282-4759insG	ENSP00000477587.1:n.282-4760_282-4759insG
NM_000348.3:c.282-4760_282-4759insG	NP_000339.2:n.282-4760_282-4759insG
XM_011533068.1:c.282-4760_282-4759insG	XP_011531370.1:n.282-4760_282-4759insG
XM_011533069.1:c.60-4760_60-4759insG	XP_011531371.1:n.60-4760_60-4759insG
XM_011533070.1:c.27-4760_27-4759insG	XP_011531372.1:n.27-4760_27-4759insG
XM_011533071.1:c.27-4760_27-4759insG	XP_011531373.1:n.27-4760_27-4759insG
XM_011533072.1:c.27-4760_27-4759insG	XP_011531374.1:n.27-4760_27-4759insG
XM_011533069.2:c.60-4760_60-4759insG	XP_011531371.1:n.60-4760_60-4759insG
XM_011533072.2:c.27-4760_27-4759insG	XP_011531374.1:n.27-4760_27-4759insG
NM_000348.4:c.282-4760_282-4759insG MANE Select	NP_000339.2:n.282-4760_282-4759insG