Canonical Allele Identifier: CA356956940

Gene: SRD5A3

Linked Data

• MyVariant Identifiers: chr4:g.56225511A>C (hg19) ; chr4:g.55359344A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359344A>C , CM000666.2:g.55359344A>C	GRCh38
NC_000004.11:g.56225511A>C , CM000666.1:g.56225511A>C	GRCh37
NC_000004.10:g.55920268A>C	NCBI36
NG_028230.1:g.18124A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.222-2A>C MANE Select	ENSP00000264228.4:n.222-2A>C
ENST00000678717.1:n.119-2A>C
ENST00000679351.1:c.222-2A>C	ENSP00000505676.1:n.222-2A>C
ENST00000679707.1:c.222-2A>C	ENSP00000505713.1:n.222-2A>C
ENST00000679836.1:c.222-2A>C	ENSP00000506601.1:n.222-2A>C
ENST00000680700.1:c.222-2A>C	ENSP00000504926.1:n.222-2A>C
ENST00000264228.8:c.222-2A>C	ENSP00000264228.4:n.222-2A>C
ENST00000505210.1:c.147-2A>C	ENSP00000424714.1:n.147-2A>C
ENST00000514398.1:n.231-2A>C
NM_024592.4:c.222-2A>C	NP_078868.1:n.222-2A>C
XM_005265766.2:c.222-2A>C	XP_005265823.1:n.222-2A>C
XM_005265767.2:c.222-2A>C	XP_005265824.1:n.222-2A>C
XM_005265766.4:c.222-2A>C	XP_005265823.1:n.222-2A>C
XM_005265767.3:c.222-2A>C	XP_005265824.1:n.222-2A>C
XM_017008601.1:c.87-2A>C	XP_016864090.1:n.87-2A>C
NM_024592.5:c.222-2A>C MANE Select	NP_078868.1:n.222-2A>C