Canonical Allele Identifier: CA1242197339

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529263_31529267delinsGAAGA , CM000664.2:g.31529263_31529267delinsGAAGA	GRCh38
NC_000002.11:g.31754333_31754337delinsGAAGA , CM000664.1:g.31754333_31754337delinsGAAGA	GRCh37
NC_000002.10:g.31607837_31607841delinsGAAGA	NCBI36
NG_008365.1:g.56705_56709delinsTCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.698+40_698+44delinsTCTTC MANE Select	ENSP00000477587.1:n.698+40_698+44delinsTCTTC
ENST00000622030.1:c.698+40_698+44delinsTCTTC	ENSP00000477587.1:n.698+40_698+44delinsTCTTC
NM_000348.3:c.698+40_698+44delinsTCTTC	NP_000339.2:n.698+40_698+44delinsTCTTC
XM_011533069.1:c.476+40_476+44delinsTCTTC	XP_011531371.1:n.476+40_476+44delinsTCTTC
XM_011533070.1:c.443+40_443+44delinsTCTTC	XP_011531372.1:n.443+40_443+44delinsTCTTC
XM_011533071.1:c.443+40_443+44delinsTCTTC	XP_011531373.1:n.443+40_443+44delinsTCTTC
XM_011533072.1:c.443+40_443+44delinsTCTTC	XP_011531374.1:n.443+40_443+44delinsTCTTC
XM_011533069.2:c.476+40_476+44delinsTCTTC	XP_011531371.1:n.476+40_476+44delinsTCTTC
XM_011533072.2:c.443+40_443+44delinsTCTTC	XP_011531374.1:n.443+40_443+44delinsTCTTC
NM_000348.4:c.698+40_698+44delinsTCTTC MANE Select	NP_000339.2:n.698+40_698+44delinsTCTTC