Canonical Allele Identifier: CA1242214602

Gene: SRD5A2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.31567432_31567433delinsTG , CM000664.2:g.31567432_31567433delinsTG	GRCh38
NC_000002.11:g.31792502_31792503delinsTG , CM000664.1:g.31792502_31792503delinsTG	GRCh37
NC_000002.10:g.31646006_31646007delinsTG	NCBI36
NG_008365.1:g.18539_18540delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622030.2:c.281+13187_281+13188delinsCA MANE Select	ENSP00000477587.1:n.281+13187_281+13188delinsCA
ENST00000622030.1:c.281+13187_281+13188delinsCA	ENSP00000477587.1:n.281+13187_281+13188delinsCA
NM_000348.3:c.281+13187_281+13188delinsCA	NP_000339.2:n.281+13187_281+13188delinsCA
XM_011533068.1:c.281+13187_281+13188delinsCA	XP_011531370.1:n.281+13187_281+13188delinsCA
XM_011533070.1:c.27-33667_27-33666delinsCA	XP_011531372.1:n.27-33667_27-33666delinsCA
XM_011533071.1:c.27-33667_27-33666delinsCA	XP_011531373.1:n.27-33667_27-33666delinsCA
XM_011533072.1:c.27-33667_27-33666delinsCA	XP_011531374.1:n.27-33667_27-33666delinsCA
XM_011533072.2:c.27-33667_27-33666delinsCA	XP_011531374.1:n.27-33667_27-33666delinsCA
NM_000348.4:c.281+13187_281+13188delinsCA MANE Select	NP_000339.2:n.281+13187_281+13188delinsCA