Canonical Allele Identifier: CA1619397250

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039962_32039963delinsTC , CM000668.2:g.32039962_32039963delinsTC	GRCh38
NC_000006.11:g.32007739_32007740delinsTC , CM000668.1:g.32007739_32007740delinsTC	GRCh37
NC_000006.10:g.32115718_32115719delinsTC	NCBI36
NG_007941.2:g.6655_6656delinsTC
NG_008337.2:g.74412_74413delinsGA
NG_007941.3:g.6658_6659delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.739-43_739-42delinsTC MANE Select	ENSP00000496625.1:n.739-43_739-42delinsTC
ENST00000418967.6:c.739-43_739-42delinsTC	ENSP00000408860.2:n.739-43_739-42delinsTC
ENST00000435122.3:c.649-43_649-42delinsTC	ENSP00000415043.2:n.649-43_649-42delinsTC
ENST00000462278.1:n.554_555delinsTC
ENST00000479074.5:n.797-43_797-42delinsTC
ENST00000479730.5:n.855-43_855-42delinsTC
ENST00000483041.5:n.908-43_908-42delinsTC
ENST00000486063.5:n.918+127_918+128delinsTC
NM_000500.7:c.739-43_739-42delinsTC	NP_000491.4:n.739-43_739-42delinsTC
NM_001128590.3:c.649-43_649-42delinsTC	NP_001122062.3:n.649-43_649-42delinsTC
XM_011514314.1:c.334-43_334-42delinsTC	XP_011512616.1:n.334-43_334-42delinsTC
NM_000500.9:c.739-43_739-42delinsTC MANE Select	NP_000491.4:n.739-43_739-42delinsTC
NM_001368143.1:c.334-43_334-42delinsTC	NP_001355072.1:n.334-43_334-42delinsTC
NM_001368144.1:c.334-43_334-42delinsTC	NP_001355073.1:n.334-43_334-42delinsTC
NM_001128590.4:c.649-43_649-42delinsTC	NP_001122062.3:n.649-43_649-42delinsTC
NM_001368143.2:c.334-43_334-42delinsTC	NP_001355072.1:n.334-43_334-42delinsTC
NM_001368144.2:c.334-43_334-42delinsTC	NP_001355073.1:n.334-43_334-42delinsTC