Canonical Allele Identifier: CA1242197323

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31529234_31529235delinsCT , CM000664.2:g.31529234_31529235delinsCT	GRCh38
NC_000002.11:g.31754304_31754305delinsCT , CM000664.1:g.31754304_31754305delinsCT	GRCh37
NC_000002.10:g.31607808_31607809delinsCT	NCBI36
NG_008365.1:g.56737_56738delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000622030.2:c.698+72_698+73delinsAG MANE Select	ENSP00000477587.1:n.698+72_698+73delinsAG...
ENST00000622030.1:c.698+72_698+73delinsAG	ENSP00000477587.1:n.698+72_698+73delinsAG...
NM_000348.3:c.698+72_698+73delinsAG	NP_000339.2:n.698+72_698+73delinsAG
XM_011533069.1:c.476+72_476+73delinsAG	XP_011531371.1:n.476+72_476+73delinsAG
XM_011533070.1:c.443+72_443+73delinsAG	XP_011531372.1:n.443+72_443+73delinsAG
XM_011533071.1:c.443+72_443+73delinsAG	XP_011531373.1:n.443+72_443+73delinsAG
XM_011533072.1:c.443+72_443+73delinsAG	XP_011531374.1:n.443+72_443+73delinsAG
XM_011533069.2:c.476+72_476+73delinsAG	XP_011531371.1:n.476+72_476+73delinsAG
XM_011533072.2:c.443+72_443+73delinsAG	XP_011531374.1:n.443+72_443+73delinsAG
NM_000348.4:c.698+72_698+73delinsAG MANE Select	NP_000339.2:n.698+72_698+73delinsAG