Canonical Allele Identifier: CA363511180

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32040577-C-A
• MyVariant Identifiers: chr6:g.32008354C>A (hg19) ; chr6:g.32040577C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040577C>A , CM000668.2:g.32040577C>A	GRCh38
NC_000006.11:g.32008354C>A , CM000668.1:g.32008354C>A	GRCh37
NC_000006.10:g.32116333C>A	NCBI36
NG_007941.2:g.7270C>A
NG_008337.2:g.73798G>T
NG_007941.3:g.7273C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1111C>A MANE Select	ENSP00000496625.1:p.Pro371Thr
ENST00000418967.6:c.1111C>A	ENSP00000408860.2:p.Pro371Thr
ENST00000435122.3:c.1021C>A	ENSP00000415043.2:p.Pro341Thr
ENST00000479074.5:n.1169C>A
ENST00000479730.5:n.1227C>A
ENST00000483041.5:n.1280C>A
ENST00000486063.5:n.1090C>A
NM_000500.7:c.1111C>A	NP_000491.4:p.Pro371Thr
NM_001128590.3:c.1021C>A	NP_001122062.3:p.Pro341Thr
XM_011514314.1:c.706C>A	XP_011512616.1:p.Pro236Thr
NM_000500.9:c.1111C>A MANE Select	NP_000491.4:p.Pro371Thr
NM_001368143.1:c.706C>A	NP_001355072.1:p.Pro236Thr
NM_001368144.1:c.706C>A	NP_001355073.1:p.Pro236Thr
NM_001128590.4:c.1021C>A	NP_001122062.3:p.Pro341Thr
NM_001368143.2:c.706C>A	NP_001355072.1:p.Pro236Thr
NM_001368144.2:c.706C>A	NP_001355073.1:p.Pro236Thr