Canonical Allele Identifier: CA363502656

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007154A>T (hg19) ; chr6:g.32039377A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039377A>T , CM000668.2:g.32039377A>T	GRCh38
NC_000006.11:g.32007154A>T , CM000668.1:g.32007154A>T	GRCh37
NC_000006.10:g.32115133A>T	NCBI36
NG_007941.2:g.6070A>T
NG_008337.2:g.74998T>A
NG_007941.3:g.6073A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.469A>T MANE Select	ENSP00000496625.1:p.Thr157Ser
ENST00000418967.6:c.469A>T	ENSP00000408860.2:p.Thr157Ser
ENST00000435122.3:c.379A>T	ENSP00000415043.2:p.Thr127Ser
ENST00000462278.1:n.57A>T
ENST00000464325.5:n.390A>T
ENST00000466779.5:c.*161A>T	ENSP00000417321.1:n.*161A>T
ENST00000466879.5:n.520A>T
ENST00000469053.5:c.*161A>T	ENSP00000418104.1:n.*161A>T
ENST00000471671.4:c.469A>T	ENSP00000418561.1:p.Thr157Ser
ENST00000478281.5:c.502A>T	ENSP00000419572.1:p.Thr168Ser
ENST00000479074.5:n.527A>T
ENST00000479730.5:n.624A>T
ENST00000483041.5:n.638A>T
ENST00000486063.5:n.649A>T
ENST00000488465.1:n.477A>T
NM_000500.7:c.469A>T	NP_000491.4:p.Thr157Ser
NM_001128590.3:c.379A>T	NP_001122062.3:p.Thr127Ser
XM_011514314.1:c.64A>T	XP_011512616.1:p.Thr22Ser
NM_000500.9:c.469A>T MANE Select	NP_000491.4:p.Thr157Ser
NM_001368143.1:c.64A>T	NP_001355072.1:p.Thr22Ser
NM_001368144.1:c.64A>T	NP_001355073.1:p.Thr22Ser
NM_001128590.4:c.379A>T	NP_001122062.3:p.Thr127Ser
NM_001368143.2:c.64A>T	NP_001355072.1:p.Thr22Ser
NM_001368144.2:c.64A>T	NP_001355073.1:p.Thr22Ser