Canonical Allele Identifier: CA2761730514

Gene: SRD5A3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55359210_55359211insTG , CM000666.2:g.55359210_55359211insTG	GRCh38
NC_000004.11:g.56225377_56225378insTG , CM000666.1:g.56225377_56225378insTG	GRCh37
NC_000004.10:g.55920134_55920135insTG	NCBI36
NG_028230.1:g.17990_17991insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264228.9:c.222-136_222-135insTG MANE Select	ENSP00000264228.4:n.222-136_222-135insTG
ENST00000678717.1:n.119-136_119-135insTG
ENST00000679351.1:c.222-136_222-135insTG	ENSP00000505676.1:n.222-136_222-135insTG
ENST00000679707.1:c.222-136_222-135insTG	ENSP00000505713.1:n.222-136_222-135insTG
ENST00000679836.1:c.222-136_222-135insTG	ENSP00000506601.1:n.222-136_222-135insTG
ENST00000680700.1:c.222-136_222-135insTG	ENSP00000504926.1:n.222-136_222-135insTG
ENST00000264228.8:c.222-136_222-135insTG	ENSP00000264228.4:n.222-136_222-135insTG
ENST00000505210.1:c.147-136_147-135insTG	ENSP00000424714.1:n.147-136_147-135insTG
ENST00000514398.1:n.211_212insTG
NM_024592.4:c.222-136_222-135insTG	NP_078868.1:n.222-136_222-135insTG
XM_005265766.2:c.222-136_222-135insTG	XP_005265823.1:n.222-136_222-135insTG
XM_005265767.2:c.222-136_222-135insTG	XP_005265824.1:n.222-136_222-135insTG
XM_005265766.4:c.222-136_222-135insTG	XP_005265823.1:n.222-136_222-135insTG
XM_005265767.3:c.222-136_222-135insTG	XP_005265824.1:n.222-136_222-135insTG
XM_017008601.1:c.87-136_87-135insTG	XP_016864090.1:n.87-136_87-135insTG
NM_024592.5:c.222-136_222-135insTG MANE Select	NP_078868.1:n.222-136_222-135insTG