Canonical Allele Identifier: CA1619396958

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039438C= , CM000668.2:g.32039438C=	GRCh38
NC_000006.11:g.32007215C= , CM000668.1:g.32007215C=	GRCh37
NC_000006.10:g.32115194C=	NCBI36
NG_007941.2:g.6131C=
NG_008337.2:g.74937G=
NG_007941.3:g.6134C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.530C= MANE Select	ENSP00000496625.1:p.Thr177=
ENST00000418967.6:c.530C=	ENSP00000408860.2:p.Thr177=
ENST00000435122.3:c.440C=	ENSP00000415043.2:p.Thr147=
ENST00000462278.1:n.118C=
ENST00000464325.5:n.451C=
ENST00000466779.5:c.*222C=	ENSP00000417321.1:n.*222C=
ENST00000466879.5:n.581C=
ENST00000469053.5:c.*222C=	ENSP00000418104.1:n.*222C=
ENST00000471671.4:c.530C=	ENSP00000418561.1:p.Thr177=
ENST00000479074.5:n.588C=
ENST00000479730.5:n.685C=
ENST00000483041.5:n.699C=
ENST00000486063.5:n.710C=
ENST00000488465.1:n.538C=
NM_000500.7:c.530C=	NP_000491.4:p.Thr177=
NM_001128590.3:c.440C=	NP_001122062.3:p.Thr147=
XM_011514314.1:c.125C=	XP_011512616.1:p.Thr42=
NM_000500.9:c.530C= MANE Select	NP_000491.4:p.Thr177=
NM_001368143.1:c.125C=	NP_001355072.1:p.Thr42=
NM_001368144.1:c.125C=	NP_001355073.1:p.Thr42=
NM_001128590.4:c.440C=	NP_001122062.3:p.Thr147=
NM_001368143.2:c.125C=	NP_001355072.1:p.Thr42=
NM_001368144.2:c.125C=	NP_001355073.1:p.Thr42=