Canonical Allele Identifier: CA363502569

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007142G>A (hg19) ; chr6:g.32039365G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039365G>A , CM000668.2:g.32039365G>A	GRCh38
NC_000006.11:g.32007142G>A , CM000668.1:g.32007142G>A	GRCh37
NC_000006.10:g.32115121G>A	NCBI36
NG_007941.2:g.6058G>A
NG_008337.2:g.75010C>T
NG_007941.3:g.6061G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.457G>A MANE Select	ENSP00000496625.1:p.Ala153Thr
ENST00000418967.6:c.457G>A	ENSP00000408860.2:p.Ala153Thr
ENST00000435122.3:c.367G>A	ENSP00000415043.2:p.Ala123Thr
ENST00000462278.1:n.45G>A
ENST00000464325.5:n.378G>A
ENST00000466779.5:c.*149G>A	ENSP00000417321.1:n.*149G>A
ENST00000466879.5:n.508G>A
ENST00000469053.5:c.*149G>A	ENSP00000418104.1:n.*149G>A
ENST00000471671.4:c.457G>A	ENSP00000418561.1:p.Ala153Thr
ENST00000478281.5:c.490G>A	ENSP00000419572.1:p.Ala164Thr
ENST00000479074.5:n.515G>A
ENST00000479730.5:n.612G>A
ENST00000483041.5:n.626G>A
ENST00000486063.5:n.637G>A
ENST00000488465.1:n.465G>A
NM_000500.7:c.457G>A	NP_000491.4:p.Ala153Thr
NM_001128590.3:c.367G>A	NP_001122062.3:p.Ala123Thr
XM_011514314.1:c.52G>A	XP_011512616.1:p.Ala18Thr
NM_000500.9:c.457G>A MANE Select	NP_000491.4:p.Ala153Thr
NM_001368143.1:c.52G>A	NP_001355072.1:p.Ala18Thr
NM_001368144.1:c.52G>A	NP_001355073.1:p.Ala18Thr
NM_001128590.4:c.367G>A	NP_001122062.3:p.Ala123Thr
NM_001368143.2:c.52G>A	NP_001355072.1:p.Ala18Thr
NM_001368144.2:c.52G>A	NP_001355073.1:p.Ala18Thr