Canonical Allele Identifier: CA1619399450

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040837_32040840delinsGCCT , CM000668.2:g.32040837_32040840delinsGCCT	GRCh38
NC_000006.11:g.32008614_32008617delinsGCCT , CM000668.1:g.32008614_32008617delinsGCCT	GRCh37
NC_000006.10:g.32116593_32116596delinsGCCT	NCBI36
NG_007941.2:g.7530_7533delinsGCCT
NG_008337.2:g.73535_73538delinsAGGC
NG_007941.3:g.7533_7536delinsGCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1223-32_1223-29delinsGCCT MANE Select	ENSP00000496625.1:n.1223-32_1223-29delins...
ENST00000418967.6:c.1223-32_1223-29delinsGCCT	ENSP00000408860.2:n.1223-32_1223-29delins...
ENST00000435122.3:c.1133-32_1133-29delinsGCCT	ENSP00000415043.2:n.1133-32_1133-29delins...
ENST00000479074.5:n.1364-32_1364-29delinsGCCT
ENST00000479730.5:n.1339-32_1339-29delinsGCCT
ENST00000483041.5:n.1392-32_1392-29delinsGCCT
ENST00000486063.5:n.1202-32_1202-29delinsGCCT
NM_000500.7:c.1223-32_1223-29delinsGCCT	NP_000491.4:n.1223-32_1223-29delinsGCCT
NM_001128590.3:c.1133-32_1133-29delinsGCCT	NP_001122062.3:n.1133-32_1133-29delinsGCC...
XM_011514314.1:c.818-32_818-29delinsGCCT	XP_011512616.1:n.818-32_818-29delinsGCCT
NM_000500.9:c.1223-32_1223-29delinsGCCT MANE Select	NP_000491.4:n.1223-32_1223-29delinsGCCT
NM_001368143.1:c.818-32_818-29delinsGCCT	NP_001355072.1:n.818-32_818-29delinsGCCT
NM_001368144.1:c.818-32_818-29delinsGCCT	NP_001355073.1:n.818-32_818-29delinsGCCT
NM_001128590.4:c.1133-32_1133-29delinsGCCT	NP_001122062.3:n.1133-32_1133-29delinsGCC...
NM_001368143.2:c.818-32_818-29delinsGCCT	NP_001355072.1:n.818-32_818-29delinsGCCT
NM_001368144.2:c.818-32_818-29delinsGCCT	NP_001355073.1:n.818-32_818-29delinsGCCT