Canonical Allele Identifier: CA439638802

Gene: SRD5A3 SRD5A3-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55370055G>C , CM000666.2:g.55370055G>C	GRCh38
NC_000004.11:g.56236222G>C , CM000666.1:g.56236222G>C	GRCh37
NC_000004.10:g.55930979G>C	NCBI36
NG_028230.1:g.28835G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_024592.5:c.921G>C (SRD5A3) MANE Select	NP_078868.1:p.Pro307=
ENST00000264228.9:c.921G>C (SRD5A3) MANE Select	ENSP00000264228.4:p.Pro307=
NM_024592.4:c.921G>C (SRD5A3)	NP_078868.1:p.Pro307=
NR_037969.1:n.364-2892C>G (SRD5A3-AS1)
ENST00000264228.8:c.921G>C (SRD5A3)	ENSP00000264228.4:p.Pro307=
ENST00000505210.1:c.513G>C (SRD5A3)	ENSP00000424714.1:p.Pro171=
ENST00000677177.2:c.768G>C (SRD5A3)
ENST00000677217.1:n.658G>C (SRD5A3)
ENST00000677930.1:n.3253G>C (SRD5A3)
ENST00000678717.1:n.818G>C (SRD5A3)
ENST00000679351.1:c.*527G>C	ENSP00000505676.1:n.*527G>C
ENST00000679707.1:c.563-1619G>C	ENSP00000505713.1:n.563-1619G>C
ENST00000679836.1:c.786G>C (SRD5A3)	ENSP00000506601.1:p.Pro262=
ENST00000680700.1:c.562+5784G>C	ENSP00000504926.1:n.562+5784G>C
XM_005265766.2:c.786G>C (SRD5A3)	XP_005265823.1:p.Pro262=
XM_005265766.4:c.786G>C (SRD5A3)	XP_005265823.1:p.Pro262=
XM_005265767.2:c.588G>C (SRD5A3)	XP_005265824.1:p.Pro196=
XM_005265767.3:c.588G>C (SRD5A3)	XP_005265824.1:p.Pro196=
XM_017008601.1:c.786G>C (SRD5A3)	XP_016864090.1:p.Pro262=