Canonical Allele Identifier: CA439526796

Gene: SRD5A3

Linked Data

• MyVariant Identifiers: chr4:g.56225570C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359403C>T , CM000666.2:g.55359403C>T	GRCh38
NC_000004.11:g.56225570C>T , CM000666.1:g.56225570C>T	GRCh37
NC_000004.10:g.55920327C>T	NCBI36
NG_028230.1:g.18183C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.279C>T MANE Select	ENSP00000264228.4:p.Cys93=
ENST00000678717.1:n.176C>T
ENST00000679351.1:c.279C>T	ENSP00000505676.1:p.Cys93=
ENST00000679707.1:c.279C>T	ENSP00000505713.1:p.Cys93=
ENST00000679836.1:c.279C>T	ENSP00000506601.1:p.Cys93=
ENST00000680700.1:c.279C>T	ENSP00000504926.1:p.Cys93=
ENST00000264228.8:c.279C>T	ENSP00000264228.4:p.Cys93=
ENST00000505210.1:c.204C>T	ENSP00000424714.1:p.Cys68=
ENST00000514398.1:n.288C>T
NM_024592.4:c.279C>T	NP_078868.1:p.Cys93=
XM_005265766.2:c.279C>T	XP_005265823.1:p.Cys93=
XM_005265767.2:c.279C>T	XP_005265824.1:p.Cys93=
XM_005265766.4:c.279C>T	XP_005265823.1:p.Cys93=
XM_005265767.3:c.279C>T	XP_005265824.1:p.Cys93=
XM_017008601.1:c.144C>T	XP_016864090.1:p.Cys48=
NM_024592.5:c.279C>T MANE Select	NP_078868.1:p.Cys93=