Canonical Allele Identifier: CA363506477

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007845C>A (hg19) ; chr6:g.32040068C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040068C>A , CM000668.2:g.32040068C>A	GRCh38
NC_000006.11:g.32007845C>A , CM000668.1:g.32007845C>A	GRCh37
NC_000006.10:g.32115824C>A	NCBI36
NG_007941.2:g.6761C>A
NG_008337.2:g.74307G>T
NG_007941.3:g.6764C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.802C>A MANE Select	ENSP00000496625.1:p.Pro268Thr
ENST00000418967.6:c.802C>A	ENSP00000408860.2:p.Pro268Thr
ENST00000435122.3:c.712C>A	ENSP00000415043.2:p.Pro238Thr
ENST00000479074.5:n.860C>A
ENST00000479730.5:n.918C>A
ENST00000483041.5:n.971C>A
ENST00000486063.5:n.918+233C>A
NM_000500.7:c.802C>A	NP_000491.4:p.Pro268Thr
NM_001128590.3:c.712C>A	NP_001122062.3:p.Pro238Thr
XM_011514314.1:c.397C>A	XP_011512616.1:p.Pro133Thr
NM_000500.9:c.802C>A MANE Select	NP_000491.4:p.Pro268Thr
NM_001368143.1:c.397C>A	NP_001355072.1:p.Pro133Thr
NM_001368144.1:c.397C>A	NP_001355073.1:p.Pro133Thr
NM_001128590.4:c.712C>A	NP_001122062.3:p.Pro238Thr
NM_001368143.2:c.397C>A	NP_001355072.1:p.Pro133Thr
NM_001368144.2:c.397C>A	NP_001355073.1:p.Pro133Thr