Canonical Allele Identifier: CA363502659

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007155C>A (hg19) ; chr6:g.32039378C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039378C>A , CM000668.2:g.32039378C>A	GRCh38
NC_000006.11:g.32007155C>A , CM000668.1:g.32007155C>A	GRCh37
NC_000006.10:g.32115134C>A	NCBI36
NG_007941.2:g.6071C>A
NG_008337.2:g.74997G>T
NG_007941.3:g.6074C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.470C>A MANE Select	ENSP00000496625.1:p.Thr157Asn
ENST00000418967.6:c.470C>A	ENSP00000408860.2:p.Thr157Asn
ENST00000435122.3:c.380C>A	ENSP00000415043.2:p.Thr127Asn
ENST00000462278.1:n.58C>A
ENST00000464325.5:n.391C>A
ENST00000466779.5:c.*162C>A	ENSP00000417321.1:n.*162C>A
ENST00000466879.5:n.521C>A
ENST00000469053.5:c.*162C>A	ENSP00000418104.1:n.*162C>A
ENST00000471671.4:c.470C>A	ENSP00000418561.1:p.Thr157Asn
ENST00000478281.5:c.503C>A	ENSP00000419572.1:p.Thr168Asn
ENST00000479074.5:n.528C>A
ENST00000479730.5:n.625C>A
ENST00000483041.5:n.639C>A
ENST00000486063.5:n.650C>A
ENST00000488465.1:n.478C>A
NM_000500.7:c.470C>A	NP_000491.4:p.Thr157Asn
NM_001128590.3:c.380C>A	NP_001122062.3:p.Thr127Asn
XM_011514314.1:c.65C>A	XP_011512616.1:p.Thr22Asn
NM_000500.9:c.470C>A MANE Select	NP_000491.4:p.Thr157Asn
NM_001368143.1:c.65C>A	NP_001355072.1:p.Thr22Asn
NM_001368144.1:c.65C>A	NP_001355073.1:p.Thr22Asn
NM_001128590.4:c.380C>A	NP_001122062.3:p.Thr127Asn
NM_001368143.2:c.65C>A	NP_001355072.1:p.Thr22Asn
NM_001368144.2:c.65C>A	NP_001355073.1:p.Thr22Asn