Canonical Allele Identifier: CA1619397437

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040372_32040373delinsTG , CM000668.2:g.32040372_32040373delinsTG	GRCh38
NC_000006.11:g.32008149_32008150delinsTG , CM000668.1:g.32008149_32008150delinsTG	GRCh37
NC_000006.10:g.32116128_32116129delinsTG	NCBI36
NG_007941.2:g.7065_7066delinsTG
NG_008337.2:g.74002_74003delinsCA
NG_007941.3:g.7068_7069delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.940-34_940-33delinsTG MANE Select	ENSP00000496625.1:n.940-34_940-33delinsTG
ENST00000418967.6:c.940-34_940-33delinsTG	ENSP00000408860.2:n.940-34_940-33delinsTG
ENST00000435122.3:c.850-34_850-33delinsTG	ENSP00000415043.2:n.850-34_850-33delinsTG
ENST00000479074.5:n.998-34_998-33delinsTG
ENST00000479730.5:n.1056-34_1056-33delinsTG
ENST00000483041.5:n.1109-34_1109-33delinsTG
ENST00000486063.5:n.919-34_919-33delinsTG
NM_000500.7:c.940-34_940-33delinsTG	NP_000491.4:n.940-34_940-33delinsTG
NM_001128590.3:c.850-34_850-33delinsTG	NP_001122062.3:n.850-34_850-33delinsTG
XM_011514314.1:c.535-34_535-33delinsTG	XP_011512616.1:n.535-34_535-33delinsTG
NM_000500.9:c.940-34_940-33delinsTG MANE Select	NP_000491.4:n.940-34_940-33delinsTG
NM_001368143.1:c.535-34_535-33delinsTG	NP_001355072.1:n.535-34_535-33delinsTG
NM_001368144.1:c.535-34_535-33delinsTG	NP_001355073.1:n.535-34_535-33delinsTG
NM_001128590.4:c.850-34_850-33delinsTG	NP_001122062.3:n.850-34_850-33delinsTG
NM_001368143.2:c.535-34_535-33delinsTG	NP_001355072.1:n.535-34_535-33delinsTG
NM_001368144.2:c.535-34_535-33delinsTG	NP_001355073.1:n.535-34_535-33delinsTG