Canonical Allele Identifier: CA1242195914

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31526152_31526158delinsTCATCAG , CM000664.2:g.31526152_31526158delinsTCATCAG	GRCh38
NC_000002.11:g.31751222_31751228delinsTCATCAG , CM000664.1:g.31751222_31751228delinsTCATCAG	GRCh37
NC_000002.10:g.31604726_31604732delinsTCATCAG	NCBI36
NG_008365.1:g.59814_59820delinsCTGATGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.*38_*44delinsCTGATGA MANE Select	ENSP00000477587.1:n.*38_*44delinsCTGATGA
ENST00000622030.1:c.*38_*44delinsCTGATGA	ENSP00000477587.1:n.*38_*44delinsCTGATGA
NM_000348.3:c.*38_*44delinsCTGATGA	NP_000339.2:n.*38_*44delinsCTGATGA
XM_011533069.1:c.*38_*44delinsCTGATGA	XP_011531371.1:n.*38_*44delinsCTGATGA
XM_011533070.1:c.*38_*44delinsCTGATGA	XP_011531372.1:n.*38_*44delinsCTGATGA
XM_011533071.1:c.*38_*44delinsCTGATGA	XP_011531373.1:n.*38_*44delinsCTGATGA
XM_011533072.1:c.*38_*44delinsCTGATGA	XP_011531374.1:n.*38_*44delinsCTGATGA
XM_011533069.2:c.*38_*44delinsCTGATGA	XP_011531371.1:n.*38_*44delinsCTGATGA
XM_011533072.2:c.*38_*44delinsCTGATGA	XP_011531374.1:n.*38_*44delinsCTGATGA
NM_000348.4:c.*38_*44delinsCTGATGA MANE Select	NP_000339.2:n.*38_*44delinsCTGATGA