Canonical Allele Identifier: CA2761730659

Gene: SRD5A3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359643_55359644insAGA , CM000666.2:g.55359643_55359644insAGA	GRCh38
NC_000004.11:g.56225810_56225811insAGA , CM000666.1:g.56225810_56225811insAGA	GRCh37
NC_000004.10:g.55920567_55920568insAGA	NCBI36
NG_028230.1:g.18423_18424insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.364+155_364+156insAGA MANE Select	ENSP00000264228.4:n.364+155_364+156insAGA
ENST00000677177.2:c.77+155_77+156insAGA
ENST00000678717.1:n.261+155_261+156insAGA
ENST00000679351.1:c.364+155_364+156insAGA	ENSP00000505676.1:n.364+155_364+156insAGA
ENST00000679707.1:c.364+155_364+156insAGA	ENSP00000505713.1:n.364+155_364+156insAGA
ENST00000679836.1:c.364+155_364+156insAGA	ENSP00000506601.1:n.364+155_364+156insAGA
ENST00000680700.1:c.364+155_364+156insAGA	ENSP00000504926.1:n.364+155_364+156insAGA
ENST00000264228.8:c.364+155_364+156insAGA	ENSP00000264228.4:n.364+155_364+156insAGA
ENST00000505210.1:c.289+155_289+156insAGA	ENSP00000424714.1:n.289+155_289+156insAGA
ENST00000514398.1:n.373+155_373+156insAGA
NM_024592.4:c.364+155_364+156insAGA	NP_078868.1:n.364+155_364+156insAGA
XM_005265766.2:c.364+155_364+156insAGA	XP_005265823.1:n.364+155_364+156insAGA
XM_005265767.2:c.364+155_364+156insAGA	XP_005265824.1:n.364+155_364+156insAGA
XM_005265766.4:c.364+155_364+156insAGA	XP_005265823.1:n.364+155_364+156insAGA
XM_005265767.3:c.364+155_364+156insAGA	XP_005265824.1:n.364+155_364+156insAGA
XM_017008601.1:c.229+155_229+156insAGA	XP_016864090.1:n.229+155_229+156insAGA
NM_024592.5:c.364+155_364+156insAGA MANE Select	NP_078868.1:n.364+155_364+156insAGA