Canonical Allele Identifier: CA1028969066

Gene: SRD5A2

Linked Data

• gnomAD v3: 2-31567476-A-ATAT
• gnomAD v4: 2-31567476-A-ATAT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567476_31567477insTAT , CM000664.2:g.31567476_31567477insTAT	GRCh38
NC_000002.11:g.31792546_31792547insTAT , CM000664.1:g.31792546_31792547insTAT	GRCh37
NC_000002.10:g.31646050_31646051insTAT	NCBI36
NG_008365.1:g.18495_18496insATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13143_281+13144insATA MANE Select	ENSP00000477587.1:n.281+13143_281+13144insATA
ENST00000622030.1:c.281+13143_281+13144insATA	ENSP00000477587.1:n.281+13143_281+13144insATA
NM_000348.3:c.281+13143_281+13144insATA	NP_000339.2:n.281+13143_281+13144insATA
XM_011533068.1:c.281+13143_281+13144insATA	XP_011531370.1:n.281+13143_281+13144insATA
XM_011533070.1:c.27-33711_27-33710insATA	XP_011531372.1:n.27-33711_27-33710insATA
XM_011533071.1:c.27-33711_27-33710insATA	XP_011531373.1:n.27-33711_27-33710insATA
XM_011533072.1:c.27-33711_27-33710insATA	XP_011531374.1:n.27-33711_27-33710insATA
XM_011533072.2:c.27-33711_27-33710insATA	XP_011531374.1:n.27-33711_27-33710insATA
NM_000348.4:c.281+13143_281+13144insATA MANE Select	NP_000339.2:n.281+13143_281+13144insATA