Canonical Allele Identifier: CA439526759

Gene: SRD5A3

Linked Data

• MyVariant Identifiers: chr4:g.56225558C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359391C>T , CM000666.2:g.55359391C>T	GRCh38
NC_000004.11:g.56225558C>T , CM000666.1:g.56225558C>T	GRCh37
NC_000004.10:g.55920315C>T	NCBI36
NG_028230.1:g.18171C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.267C>T MANE Select	ENSP00000264228.4:p.Phe89=
ENST00000678717.1:n.164C>T
ENST00000679351.1:c.267C>T	ENSP00000505676.1:p.Phe89=
ENST00000679707.1:c.267C>T	ENSP00000505713.1:p.Phe89=
ENST00000679836.1:c.267C>T	ENSP00000506601.1:p.Phe89=
ENST00000680700.1:c.267C>T	ENSP00000504926.1:p.Phe89=
ENST00000264228.8:c.267C>T	ENSP00000264228.4:p.Phe89=
ENST00000505210.1:c.192C>T	ENSP00000424714.1:p.Phe64=
ENST00000514398.1:n.276C>T
NM_024592.4:c.267C>T	NP_078868.1:p.Phe89=
XM_005265766.2:c.267C>T	XP_005265823.1:p.Phe89=
XM_005265767.2:c.267C>T	XP_005265824.1:p.Phe89=
XM_005265766.4:c.267C>T	XP_005265823.1:p.Phe89=
XM_005265767.3:c.267C>T	XP_005265824.1:p.Phe89=
XM_017008601.1:c.132C>T	XP_016864090.1:p.Phe44=
NM_024592.5:c.267C>T MANE Select	NP_078868.1:p.Phe89=