Canonical Allele Identifier: CA356957200

Gene: SRD5A3

Linked Data

• MyVariant Identifiers: chr4:g.56225630A>C (hg19) ; chr4:g.55359463A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359463A>C , CM000666.2:g.55359463A>C	GRCh38
NC_000004.11:g.56225630A>C , CM000666.1:g.56225630A>C	GRCh37
NC_000004.10:g.55920387A>C	NCBI36
NG_028230.1:g.18243A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.339A>C MANE Select	ENSP00000264228.4:p.Arg113Ser
ENST00000677177.2:c.52A>C
ENST00000678717.1:n.236A>C
ENST00000679351.1:c.339A>C	ENSP00000505676.1:p.Arg113Ser
ENST00000679707.1:c.339A>C	ENSP00000505713.1:p.Arg113Ser
ENST00000679836.1:c.339A>C	ENSP00000506601.1:p.Arg113Ser
ENST00000680700.1:c.339A>C	ENSP00000504926.1:p.Arg113Ser
ENST00000264228.8:c.339A>C	ENSP00000264228.4:p.Arg113Ser
ENST00000505210.1:c.264A>C	ENSP00000424714.1:p.Arg88Ser
ENST00000514398.1:n.348A>C
NM_024592.4:c.339A>C	NP_078868.1:p.Arg113Ser
XM_005265766.2:c.339A>C	XP_005265823.1:p.Arg113Ser
XM_005265767.2:c.339A>C	XP_005265824.1:p.Arg113Ser
XM_005265766.4:c.339A>C	XP_005265823.1:p.Arg113Ser
XM_005265767.3:c.339A>C	XP_005265824.1:p.Arg113Ser
XM_017008601.1:c.204A>C	XP_016864090.1:p.Arg68Ser
NM_024592.5:c.339A>C MANE Select	NP_078868.1:p.Arg113Ser