Canonical Allele Identifier: CA363500919

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32006903T>G (hg19) ; chr6:g.32039126T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039126T>G , CM000668.2:g.32039126T>G	GRCh38
NC_000006.11:g.32006903T>G , CM000668.1:g.32006903T>G	GRCh37
NC_000006.10:g.32114882T>G	NCBI36
NG_007941.2:g.5819T>G
NG_007941.3:g.5822T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.325T>G MANE Select	ENSP00000496625.1:p.Ser109Ala
ENST00000418967.6:c.325T>G	ENSP00000408860.2:p.Ser109Ala
ENST00000435122.3:c.235T>G	ENSP00000415043.2:p.Ser79Ala
ENST00000464325.5:n.246T>G
ENST00000466779.5:c.*17T>G	ENSP00000417321.1:n.*17T>G
ENST00000466879.5:n.376T>G
ENST00000469053.5:c.*17T>G	ENSP00000418104.1:n.*17T>G
ENST00000471671.4:c.325T>G	ENSP00000418561.1:p.Ser109Ala
ENST00000478281.5:c.358T>G	ENSP00000419572.1:p.Ser120Ala
ENST00000479074.5:n.383T>G
ENST00000479730.5:n.480T>G
ENST00000483041.5:n.494T>G
ENST00000486063.5:n.505T>G
ENST00000488465.1:n.333T>G
NM_000500.7:c.325T>G	NP_000491.4:p.Ser109Ala
NM_001128590.3:c.235T>G	NP_001122062.3:p.Ser79Ala
XM_011514314.1:c.-81T>G	XP_011512616.1:n.-81T>G
NM_000500.9:c.325T>G MANE Select	NP_000491.4:p.Ser109Ala
NM_001368143.1:c.-81T>G	NP_001355072.1:n.-81T>G
NM_001368144.1:c.-81T>G	NP_001355073.1:n.-81T>G
NM_001128590.4:c.235T>G	NP_001122062.3:p.Ser79Ala
NM_001368143.2:c.-81T>G	NP_001355072.1:n.-81T>G
NM_001368144.2:c.-81T>G	NP_001355073.1:n.-81T>G