Canonical Allele Identifier: CA363503133

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007215C>T (hg19) ; chr6:g.32039438C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.530C>T MANE Select	ENSP00000496625.1:p.Thr177Ile
ENST00000418967.6:c.530C>T	ENSP00000408860.2:p.Thr177Ile
ENST00000435122.3:c.440C>T	ENSP00000415043.2:p.Thr147Ile
ENST00000462278.1:n.118C>T
ENST00000464325.5:n.451C>T
ENST00000466779.5:c.*222C>T	ENSP00000417321.1:n.*222C>T
ENST00000466879.5:n.581C>T
ENST00000469053.5:c.*222C>T	ENSP00000418104.1:n.*222C>T
ENST00000471671.4:c.530C>T	ENSP00000418561.1:p.Thr177Ile
ENST00000479074.5:n.588C>T
ENST00000479730.5:n.685C>T
ENST00000483041.5:n.699C>T
ENST00000486063.5:n.710C>T
ENST00000488465.1:n.538C>T
NM_000500.7:c.530C>T	NP_000491.4:p.Thr177Ile
NM_001128590.3:c.440C>T	NP_001122062.3:p.Thr147Ile
XM_011514314.1:c.125C>T	XP_011512616.1:p.Thr42Ile
NM_000500.9:c.530C>T MANE Select	NP_000491.4:p.Thr177Ile
NM_001368143.1:c.125C>T	NP_001355072.1:p.Thr42Ile
NM_001368144.1:c.125C>T	NP_001355073.1:p.Thr42Ile
NM_001128590.4:c.440C>T	NP_001122062.3:p.Thr147Ile
NM_001368143.2:c.125C>T	NP_001355072.1:p.Thr42Ile
NM_001368144.2:c.125C>T	NP_001355073.1:p.Thr42Ile