Canonical Allele Identifier: CA823931869

Gene: CYP21A2

Linked Data

• dbSNP Id: rs779360081
• gnomAD v4: 6-32040777-TG-T
• MyVariant Identifiers: chr6:g.32008555del (hg19) ; chr6:g.32040778del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040783del , CM000668.2:g.32040783del	GRCh38
NC_000006.11:g.32008560del , CM000668.1:g.32008560del	GRCh37
NC_000006.10:g.32116539del	NCBI36
NG_007941.2:g.7476del
NG_008337.2:g.73597del
NG_007941.3:g.7479del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1222+12del MANE Select	ENSP00000496625.1:n.1222+12del
ENST00000418967.6:c.1222+12del	ENSP00000408860.2:n.1222+12del
ENST00000435122.3:c.1132+12del	ENSP00000415043.2:n.1132+12del
ENST00000479074.5:n.1363+12del
ENST00000479730.5:n.1338+12del
ENST00000483041.5:n.1391+12del
ENST00000486063.5:n.1201+12del
NM_000500.7:c.1222+12del	NP_000491.4:n.1222+12del
NM_001128590.3:c.1132+12del	NP_001122062.3:n.1132+12del
XM_011514314.1:c.817+12del	XP_011512616.1:n.817+12del
NM_000500.9:c.1222+12del MANE Select	NP_000491.4:n.1222+12del
NM_001368143.1:c.817+12del	NP_001355072.1:n.817+12del
NM_001368144.1:c.817+12del	NP_001355073.1:n.817+12del
NM_001128590.4:c.1132+12del	NP_001122062.3:n.1132+12del
NM_001368143.2:c.817+12del	NP_001355072.1:n.817+12del
NM_001368144.2:c.817+12del	NP_001355073.1:n.817+12del