Canonical Allele Identifier: CA1242214680

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567550_31567555delinsCAACAA , CM000664.2:g.31567550_31567555delinsCAACAA	GRCh38
NC_000002.11:g.31792620_31792625delinsCAACAA , CM000664.1:g.31792620_31792625delinsCAACAA	GRCh37
NC_000002.10:g.31646124_31646129delinsCAACAA	NCBI36
NG_008365.1:g.18417_18422delinsTTGTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13065_281+13070delinsTTGTTG MANE Select	ENSP00000477587.1:n.281+13065_281+13070delinsTTGTTG
ENST00000622030.1:c.281+13065_281+13070delinsTTGTTG	ENSP00000477587.1:n.281+13065_281+13070delinsTTGTTG
NM_000348.3:c.281+13065_281+13070delinsTTGTTG	NP_000339.2:n.281+13065_281+13070delinsTTGTTG
XM_011533068.1:c.281+13065_281+13070delinsTTGTTG	XP_011531370.1:n.281+13065_281+13070delinsTTGTTG
XM_011533070.1:c.27-33789_27-33784delinsTTGTTG	XP_011531372.1:n.27-33789_27-33784delinsTTGTTG
XM_011533071.1:c.27-33789_27-33784delinsTTGTTG	XP_011531373.1:n.27-33789_27-33784delinsTTGTTG
XM_011533072.1:c.27-33789_27-33784delinsTTGTTG	XP_011531374.1:n.27-33789_27-33784delinsTTGTTG
XM_011533072.2:c.27-33789_27-33784delinsTTGTTG	XP_011531374.1:n.27-33789_27-33784delinsTTGTTG
NM_000348.4:c.281+13065_281+13070delinsTTGTTG MANE Select	NP_000339.2:n.281+13065_281+13070delinsTTGTTG