Canonical Allele Identifier: CA363504302

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007416T>A (hg19) ; chr6:g.32039639T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039639T>A , CM000668.2:g.32039639T>A	GRCh38
NC_000006.11:g.32007416T>A , CM000668.1:g.32007416T>A	GRCh37
NC_000006.10:g.32115395T>A	NCBI36
NG_007941.2:g.6332T>A
NG_008337.2:g.74736A>T
NG_007941.3:g.6335T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.643T>A MANE Select	ENSP00000496625.1:p.Phe215Ile
ENST00000418967.6:c.643T>A	ENSP00000408860.2:p.Phe215Ile
ENST00000435122.3:c.553T>A	ENSP00000415043.2:p.Phe185Ile
ENST00000462278.1:n.231T>A
ENST00000464325.5:n.564T>A
ENST00000466779.5:c.*335T>A	ENSP00000417321.1:n.*335T>A
ENST00000466879.5:n.694T>A
ENST00000469053.5:c.*335T>A	ENSP00000418104.1:n.*335T>A
ENST00000479074.5:n.701T>A
ENST00000479730.5:n.759T>A
ENST00000483041.5:n.812T>A
ENST00000486063.5:n.823T>A
NM_000500.7:c.643T>A	NP_000491.4:p.Phe215Ile
NM_001128590.3:c.553T>A	NP_001122062.3:p.Phe185Ile
XM_011514314.1:c.238T>A	XP_011512616.1:p.Phe80Ile
NM_000500.9:c.643T>A MANE Select	NP_000491.4:p.Phe215Ile
NM_001368143.1:c.238T>A	NP_001355072.1:p.Phe80Ile
NM_001368144.1:c.238T>A	NP_001355073.1:p.Phe80Ile
NM_001128590.4:c.553T>A	NP_001122062.3:p.Phe185Ile
NM_001368143.2:c.238T>A	NP_001355072.1:p.Phe80Ile
NM_001368144.2:c.238T>A	NP_001355073.1:p.Phe80Ile