Canonical Allele Identifier: CA356956958

Gene: SRD5A3

Linked Data

• MyVariant Identifiers: chr4:g.56225517T>G (hg19) ; chr4:g.55359350T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359350T>G , CM000666.2:g.55359350T>G	GRCh38
NC_000004.11:g.56225517T>G , CM000666.1:g.56225517T>G	GRCh37
NC_000004.10:g.55920274T>G	NCBI36
NG_028230.1:g.18130T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.226T>G MANE Select	ENSP00000264228.4:p.Phe76Val
ENST00000678717.1:n.123T>G
ENST00000679351.1:c.226T>G	ENSP00000505676.1:p.Phe76Val
ENST00000679707.1:c.226T>G	ENSP00000505713.1:p.Phe76Val
ENST00000679836.1:c.226T>G	ENSP00000506601.1:p.Phe76Val
ENST00000680700.1:c.226T>G	ENSP00000504926.1:p.Phe76Val
ENST00000264228.8:c.226T>G	ENSP00000264228.4:p.Phe76Val
ENST00000505210.1:c.151T>G	ENSP00000424714.1:p.Phe51Val
ENST00000514398.1:n.235T>G
NM_024592.4:c.226T>G	NP_078868.1:p.Phe76Val
XM_005265766.2:c.226T>G	XP_005265823.1:p.Phe76Val
XM_005265767.2:c.226T>G	XP_005265824.1:p.Phe76Val
XM_005265766.4:c.226T>G	XP_005265823.1:p.Phe76Val
XM_005265767.3:c.226T>G	XP_005265824.1:p.Phe76Val
XM_017008601.1:c.91T>G	XP_016864090.1:p.Phe31Val
NM_024592.5:c.226T>G MANE Select	NP_078868.1:p.Phe76Val