Canonical Allele Identifier: CA1242198377

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531528_31531529delinsGC , CM000664.2:g.31531528_31531529delinsGC	GRCh38
NC_000002.11:g.31756598_31756599delinsGC , CM000664.1:g.31756598_31756599delinsGC	GRCh37
NC_000002.10:g.31610102_31610103delinsGC	NCBI36
NG_008365.1:g.54443_54444delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.446-57_446-56delinsGC MANE Select	ENSP00000477587.1:n.446-57_446-56delinsGC
ENST00000622030.1:c.446-57_446-56delinsGC	ENSP00000477587.1:n.446-57_446-56delinsGC
NM_000348.3:c.446-57_446-56delinsGC	NP_000339.2:n.446-57_446-56delinsGC
XM_011533069.1:c.224-57_224-56delinsGC	XP_011531371.1:n.224-57_224-56delinsGC
XM_011533070.1:c.191-57_191-56delinsGC	XP_011531372.1:n.191-57_191-56delinsGC
XM_011533071.1:c.191-57_191-56delinsGC	XP_011531373.1:n.191-57_191-56delinsGC
XM_011533072.1:c.191-57_191-56delinsGC	XP_011531374.1:n.191-57_191-56delinsGC
XM_011533069.2:c.224-57_224-56delinsGC	XP_011531371.1:n.224-57_224-56delinsGC
XM_011533072.2:c.191-57_191-56delinsGC	XP_011531374.1:n.191-57_191-56delinsGC
NM_000348.4:c.446-57_446-56delinsGC MANE Select	NP_000339.2:n.446-57_446-56delinsGC