Canonical Allele Identifier: CA97481811

Gene: SRD5A3 SRD5A3-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55370133C>T , CM000666.2:g.55370133C>T	GRCh38
NC_000004.11:g.56236300C>T , CM000666.1:g.56236300C>T	GRCh37
NC_000004.10:g.55931057C>T	NCBI36
NG_028230.1:g.28913C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_024592.5:c.*42C>T (SRD5A3) MANE Select	NP_078868.1:n.*42C>T
ENST00000264228.9:c.*42C>T (SRD5A3) MANE Select	ENSP00000264228.4:n.*42C>T
NM_024592.4:c.*42C>T (SRD5A3)	NP_078868.1:n.*42C>T
NR_037969.1:n.364-2970G>A (SRD5A3-AS1)
ENST00000264228.8:c.*42C>T (SRD5A3)	ENSP00000264228.4:n.*42C>T
ENST00000505210.1:c.591C>T (SRD5A3)	ENSP00000424714.1:n.591C>T
ENST00000677217.1:n.736C>T (SRD5A3)
ENST00000677930.1:n.3331C>T (SRD5A3)
ENST00000678717.1:n.896C>T (SRD5A3)
ENST00000679351.1:c.*605C>T	ENSP00000505676.1:n.*605C>T
ENST00000679707.1:c.563-1541C>T	ENSP00000505713.1:n.563-1541C>T
ENST00000679836.1:c.*42C>T (SRD5A3)	ENSP00000506601.1:n.*42C>T
ENST00000680700.1:c.562+5862C>T	ENSP00000504926.1:n.562+5862C>T
XM_005265766.2:c.*42C>T (SRD5A3)	XP_005265823.1:n.*42C>T
XM_005265766.4:c.*42C>T (SRD5A3)	XP_005265823.1:n.*42C>T
XM_005265767.2:c.*42C>T (SRD5A3)	XP_005265824.1:n.*42C>T
XM_005265767.3:c.*42C>T (SRD5A3)	XP_005265824.1:n.*42C>T
XM_017008601.1:c.*42C>T (SRD5A3)	XP_016864090.1:n.*42C>T