Canonical Allele Identifier: CA449729745

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007898T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040121T>A , CM000668.2:g.32040121T>A	GRCh38
NC_000006.11:g.32007898T>A , CM000668.1:g.32007898T>A	GRCh37
NC_000006.10:g.32115877T>A	NCBI36
NG_007941.2:g.6814T>A
NG_008337.2:g.74254A>T
NG_007941.3:g.6817T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.855T>A MANE Select	ENSP00000496625.1:p.Ala285=
ENST00000418967.6:c.855T>A	ENSP00000408860.2:p.Ala285=
ENST00000435122.3:c.765T>A	ENSP00000415043.2:p.Ala255=
ENST00000479074.5:n.913T>A
ENST00000479730.5:n.971T>A
ENST00000483041.5:n.1024T>A
ENST00000486063.5:n.919-285T>A
NM_000500.7:c.855T>A	NP_000491.4:p.Ala285=
NM_001128590.3:c.765T>A	NP_001122062.3:p.Ala255=
XM_011514314.1:c.450T>A	XP_011512616.1:p.Ala150=
NM_000500.9:c.855T>A MANE Select	NP_000491.4:p.Ala285=
NM_001368143.1:c.450T>A	NP_001355072.1:p.Ala150=
NM_001368144.1:c.450T>A	NP_001355073.1:p.Ala150=
NM_001128590.4:c.765T>A	NP_001122062.3:p.Ala255=
NM_001368143.2:c.450T>A	NP_001355072.1:p.Ala150=
NM_001368144.2:c.450T>A	NP_001355073.1:p.Ala150=