Canonical Allele Identifier: CA45140567

Gene: SRD5A2

Linked Data

• dbSNP Id: rs71247601
• MyVariant Identifiers: chr2:g.31792524_31792525insGTG (hg19) ; chr2:g.31567454_31567455insGTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567452_31567454dup , CM000664.2:g.31567452_31567454dup	GRCh38
NC_000002.11:g.31792522_31792524dup , CM000664.1:g.31792522_31792524dup	GRCh37
NC_000002.10:g.31646026_31646028dup	NCBI36
NG_008365.1:g.18518_18520dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13166_281+13168dup MANE Select	ENSP00000477587.1:n.281+13166_281+13168dup
ENST00000622030.1:c.281+13166_281+13168dup	ENSP00000477587.1:n.281+13166_281+13168dup
NM_000348.3:c.281+13166_281+13168dup	NP_000339.2:n.281+13166_281+13168dup
XM_011533068.1:c.281+13166_281+13168dup	XP_011531370.1:n.281+13166_281+13168dup
XM_011533070.1:c.27-33688_27-33686dup	XP_011531372.1:n.27-33688_27-33686dup
XM_011533071.1:c.27-33688_27-33686dup	XP_011531373.1:n.27-33688_27-33686dup
XM_011533072.1:c.27-33688_27-33686dup	XP_011531374.1:n.27-33688_27-33686dup
XM_011533072.2:c.27-33688_27-33686dup	XP_011531374.1:n.27-33688_27-33686dup
NM_000348.4:c.281+13166_281+13168dup MANE Select	NP_000339.2:n.281+13166_281+13168dup