Canonical Allele Identifier: CA2749374957

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526576_31526578dup , CM000664.2:g.31526576_31526578dup	GRCh38
NC_000002.11:g.31751646_31751648dup , CM000664.1:g.31751646_31751648dup	GRCh37
NC_000002.10:g.31605150_31605152dup	NCBI36
NG_008365.1:g.59395_59397dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-315_699-313dup MANE Select	ENSP00000477587.1:n.699-315_699-313dup
ENST00000622030.1:c.699-315_699-313dup	ENSP00000477587.1:n.699-315_699-313dup
NM_000348.3:c.699-315_699-313dup	NP_000339.2:n.699-315_699-313dup
XM_011533069.1:c.477-315_477-313dup	XP_011531371.1:n.477-315_477-313dup
XM_011533070.1:c.444-315_444-313dup	XP_011531372.1:n.444-315_444-313dup
XM_011533071.1:c.444-315_444-313dup	XP_011531373.1:n.444-315_444-313dup
XM_011533072.1:c.444-315_444-313dup	XP_011531374.1:n.444-315_444-313dup
XM_011533069.2:c.477-315_477-313dup	XP_011531371.1:n.477-315_477-313dup
XM_011533072.2:c.444-315_444-313dup	XP_011531374.1:n.444-315_444-313dup
NM_000348.4:c.699-315_699-313dup MANE Select	NP_000339.2:n.699-315_699-313dup