Canonical Allele Identifier: CA356957069

Gene: SRD5A3

Linked Data

• gnomAD v4: 4-55359401-T-C
• MyVariant Identifiers: chr4:g.56225568T>C (hg19) ; chr4:g.55359401T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359401T>C , CM000666.2:g.55359401T>C	GRCh38
NC_000004.11:g.56225568T>C , CM000666.1:g.56225568T>C	GRCh37
NC_000004.10:g.55920325T>C	NCBI36
NG_028230.1:g.18181T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.277T>C MANE Select	ENSP00000264228.4:p.Cys93Arg
ENST00000678717.1:n.174T>C
ENST00000679351.1:c.277T>C	ENSP00000505676.1:p.Cys93Arg
ENST00000679707.1:c.277T>C	ENSP00000505713.1:p.Cys93Arg
ENST00000679836.1:c.277T>C	ENSP00000506601.1:p.Cys93Arg
ENST00000680700.1:c.277T>C	ENSP00000504926.1:p.Cys93Arg
ENST00000264228.8:c.277T>C	ENSP00000264228.4:p.Cys93Arg
ENST00000505210.1:c.202T>C	ENSP00000424714.1:p.Cys68Arg
ENST00000514398.1:n.286T>C
NM_024592.4:c.277T>C	NP_078868.1:p.Cys93Arg
XM_005265766.2:c.277T>C	XP_005265823.1:p.Cys93Arg
XM_005265767.2:c.277T>C	XP_005265824.1:p.Cys93Arg
XM_005265766.4:c.277T>C	XP_005265823.1:p.Cys93Arg
XM_005265767.3:c.277T>C	XP_005265824.1:p.Cys93Arg
XM_017008601.1:c.142T>C	XP_016864090.1:p.Cys48Arg
NM_024592.5:c.277T>C MANE Select	NP_078868.1:p.Cys93Arg