Canonical Allele Identifier: CA1242198221

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31531201_31531204delinsAAAT , CM000664.2:g.31531201_31531204delinsAAAT	GRCh38
NC_000002.11:g.31756271_31756274delinsAAAT , CM000664.1:g.31756271_31756274delinsAAAT	GRCh37
NC_000002.10:g.31609775_31609778delinsAAAT	NCBI36
NG_008365.1:g.54768_54771delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.547+167_547+170delinsATTT MANE Select	ENSP00000477587.1:n.547+167_547+170delinsATTT
ENST00000622030.1:c.547+167_547+170delinsATTT	ENSP00000477587.1:n.547+167_547+170delinsATTT
NM_000348.3:c.547+167_547+170delinsATTT	NP_000339.2:n.547+167_547+170delinsATTT
XM_011533069.1:c.325+167_325+170delinsATTT	XP_011531371.1:n.325+167_325+170delinsATTT
XM_011533070.1:c.292+167_292+170delinsATTT	XP_011531372.1:n.292+167_292+170delinsATTT
XM_011533071.1:c.292+167_292+170delinsATTT	XP_011531373.1:n.292+167_292+170delinsATTT
XM_011533072.1:c.292+167_292+170delinsATTT	XP_011531374.1:n.292+167_292+170delinsATTT
XM_011533069.2:c.325+167_325+170delinsATTT	XP_011531371.1:n.325+167_325+170delinsATTT
XM_011533072.2:c.292+167_292+170delinsATTT	XP_011531374.1:n.292+167_292+170delinsATTT
NM_000348.4:c.547+167_547+170delinsATTT MANE Select	NP_000339.2:n.547+167_547+170delinsATTT