Canonical Allele Identifier: CA1242196085

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526559_31526560delinsAT , CM000664.2:g.31526559_31526560delinsAT	GRCh38
NC_000002.11:g.31751629_31751630delinsAT , CM000664.1:g.31751629_31751630delinsAT	GRCh37
NC_000002.10:g.31605133_31605134delinsAT	NCBI36
NG_008365.1:g.59412_59413delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-298_699-297delinsAT MANE Select	ENSP00000477587.1:n.699-298_699-297delinsAT
ENST00000622030.1:c.699-298_699-297delinsAT	ENSP00000477587.1:n.699-298_699-297delinsAT
NM_000348.3:c.699-298_699-297delinsAT	NP_000339.2:n.699-298_699-297delinsAT
XM_011533069.1:c.477-298_477-297delinsAT	XP_011531371.1:n.477-298_477-297delinsAT
XM_011533070.1:c.444-298_444-297delinsAT	XP_011531372.1:n.444-298_444-297delinsAT
XM_011533071.1:c.444-298_444-297delinsAT	XP_011531373.1:n.444-298_444-297delinsAT
XM_011533072.1:c.444-298_444-297delinsAT	XP_011531374.1:n.444-298_444-297delinsAT
XM_011533069.2:c.477-298_477-297delinsAT	XP_011531371.1:n.477-298_477-297delinsAT
XM_011533072.2:c.444-298_444-297delinsAT	XP_011531374.1:n.444-298_444-297delinsAT
NM_000348.4:c.699-298_699-297delinsAT MANE Select	NP_000339.2:n.699-298_699-297delinsAT