Canonical Allele Identifier: CA1242220997

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31580603_31580604delinsCA , CM000664.2:g.31580603_31580604delinsCA	GRCh38
NC_000002.11:g.31805673_31805674delinsCA , CM000664.1:g.31805673_31805674delinsCA	GRCh37
NC_000002.10:g.31659177_31659178delinsCA	NCBI36
NG_008365.1:g.5368_5369delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+16_281+17delinsTG MANE Select	ENSP00000477587.1:n.281+16_281+17delinsTG
ENST00000622030.1:c.281+16_281+17delinsTG	ENSP00000477587.1:n.281+16_281+17delinsTG
NM_000348.3:c.281+16_281+17delinsTG	NP_000339.2:n.281+16_281+17delinsTG
XM_011533068.1:c.281+16_281+17delinsTG	XP_011531370.1:n.281+16_281+17delinsTG
XM_011533070.1:c.27-46838_27-46837delinsTG	XP_011531372.1:n.27-46838_27-46837delinsTG
XM_011533071.1:c.27-46838_27-46837delinsTG	XP_011531373.1:n.27-46838_27-46837delinsTG
XM_011533072.1:c.27-46838_27-46837delinsTG	XP_011531374.1:n.27-46838_27-46837delinsTG
XM_011533072.2:c.27-46838_27-46837delinsTG	XP_011531374.1:n.27-46838_27-46837delinsTG
NM_000348.4:c.281+16_281+17delinsTG MANE Select	NP_000339.2:n.281+16_281+17delinsTG