Canonical Allele Identifier: CA1242196093

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526579_31526580delinsAC , CM000664.2:g.31526579_31526580delinsAC	GRCh38
NC_000002.11:g.31751649_31751650delinsAC , CM000664.1:g.31751649_31751650delinsAC	GRCh37
NC_000002.10:g.31605153_31605154delinsAC	NCBI36
NG_008365.1:g.59392_59393delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.699-318_699-317delinsGT MANE Select	ENSP00000477587.1:n.699-318_699-317delinsGT
ENST00000622030.1:c.699-318_699-317delinsGT	ENSP00000477587.1:n.699-318_699-317delinsGT
NM_000348.3:c.699-318_699-317delinsGT	NP_000339.2:n.699-318_699-317delinsGT
XM_011533069.1:c.477-318_477-317delinsGT	XP_011531371.1:n.477-318_477-317delinsGT
XM_011533070.1:c.444-318_444-317delinsGT	XP_011531372.1:n.444-318_444-317delinsGT
XM_011533071.1:c.444-318_444-317delinsGT	XP_011531373.1:n.444-318_444-317delinsGT
XM_011533072.1:c.444-318_444-317delinsGT	XP_011531374.1:n.444-318_444-317delinsGT
XM_011533069.2:c.477-318_477-317delinsGT	XP_011531371.1:n.477-318_477-317delinsGT
XM_011533072.2:c.444-318_444-317delinsGT	XP_011531374.1:n.444-318_444-317delinsGT
NM_000348.4:c.699-318_699-317delinsGT MANE Select	NP_000339.2:n.699-318_699-317delinsGT