Canonical Allele Identifier: CA767779461

Gene: SRD5A2

Linked Data

• dbSNP Id: rs1433536529
• MyVariant Identifiers: chr2:g.31792639del (hg19) ; chr2:g.31567569del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567571del , CM000664.2:g.31567571del	GRCh38
NC_000002.11:g.31792641del , CM000664.1:g.31792641del	GRCh37
NC_000002.10:g.31646145del	NCBI36
NG_008365.1:g.18403del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13051del MANE Select	ENSP00000477587.1:n.281+13051del
ENST00000622030.1:c.281+13051del	ENSP00000477587.1:n.281+13051del
NM_000348.3:c.281+13051del	NP_000339.2:n.281+13051del
XM_011533068.1:c.281+13051del	XP_011531370.1:n.281+13051del
XM_011533070.1:c.27-33803del	XP_011531372.1:n.27-33803del
XM_011533071.1:c.27-33803del	XP_011531373.1:n.27-33803del
XM_011533072.1:c.27-33803del	XP_011531374.1:n.27-33803del
XM_011533072.2:c.27-33803del	XP_011531374.1:n.27-33803del
NM_000348.4:c.281+13051del MANE Select	NP_000339.2:n.281+13051del