Canonical Allele Identifier: CA1619399572

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32041018_32041036delinsGCCCTGCCCTCCCTGCAGC , CM000668.2:g.32041018_32041036delinsGCCCTGCCCTCCCTGCAGC	GRCh38
NC_000006.11:g.32008795_32008813delinsGCCCTGCCCTCCCTGCAGC , CM000668.1:g.32008795_32008813delinsGCCCTGCCCTCCCTGCAGC	GRCh37
NC_000006.10:g.32116774_32116792delinsGCCCTGCCCTCCCTGCAGC	NCBI36
NG_007941.2:g.7711_7729delinsGCCCTGCCCTCCCTGCAGC
NG_008337.2:g.73339_73357delinsGCTGCAGGGAGGGCAGGGC
NG_007941.3:g.7714_7732delinsGCCCTGCCCTCCCTGCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.1372_1390delinsGCCCTGCCCTCCCTGCAGC MANE Select	ENSP00000496625.1:p.Ala458=
ENST00000418967.6:c.1372_1390delinsGCCCTGCCCTCCCTGCAGC	ENSP00000408860.2:p.Ala458=
ENST00000435122.3:c.1282_1300delinsGCCCTGCCCTCCCTGCAGC	ENSP00000415043.2:p.Ala428=
ENST00000479074.5:n.1513_1531delinsGCCCTGCCCTCCCTGCAGC
ENST00000479730.5:n.1488_1506delinsGCCCTGCCCTCCCTGCAGC
ENST00000483041.5:n.1541_1559delinsGCCCTGCCCTCCCTGCAGC
ENST00000486063.5:n.1351_1369delinsGCCCTGCCCTCCCTGCAGC
NM_000500.7:c.1372_1390delinsGCCCTGCCCTCCCTGCAGC	NP_000491.4:p.Ala458=
NM_001128590.3:c.1282_1300delinsGCCCTGCCCTCCCTGCAGC	NP_001122062.3:p.Ala428=
XM_011514314.1:c.967_985delinsGCCCTGCCCTCCCTGCAGC	XP_011512616.1:p.Ala323=
NM_000500.9:c.1372_1390delinsGCCCTGCCCTCCCTGCAGC MANE Select	NP_000491.4:p.Ala458=
NM_001368143.1:c.967_985delinsGCCCTGCCCTCCCTGCAGC	NP_001355072.1:p.Ala323=
NM_001368144.1:c.967_985delinsGCCCTGCCCTCCCTGCAGC	NP_001355073.1:p.Ala323=
NM_001128590.4:c.1282_1300delinsGCCCTGCCCTCCCTGCAGC	NP_001122062.3:p.Ala428=
NM_001368143.2:c.967_985delinsGCCCTGCCCTCCCTGCAGC	NP_001355072.1:p.Ala323=
NM_001368144.2:c.967_985delinsGCCCTGCCCTCCCTGCAGC	NP_001355073.1:p.Ala323=