Canonical Allele Identifier: CA363501749

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32006994T>C (hg19) ; chr6:g.32039217T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039217T>C , CM000668.2:g.32039217T>C	GRCh38
NC_000006.11:g.32006994T>C , CM000668.1:g.32006994T>C	GRCh37
NC_000006.10:g.32114973T>C	NCBI36
NG_007941.2:g.5910T>C
NG_008337.2:g.75158A>G
NG_007941.3:g.5913T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.416T>C MANE Select	ENSP00000496625.1:p.Val139Ala
ENST00000418967.6:c.416T>C	ENSP00000408860.2:p.Val139Ala
ENST00000435122.3:c.326T>C	ENSP00000415043.2:p.Val109Ala
ENST00000462278.1:n.4T>C
ENST00000464325.5:n.337T>C
ENST00000466779.5:c.*108T>C	ENSP00000417321.1:n.*108T>C
ENST00000466879.5:n.467T>C
ENST00000469053.5:c.*108T>C	ENSP00000418104.1:n.*108T>C
ENST00000471671.4:c.416T>C	ENSP00000418561.1:p.Val139Ala
ENST00000478281.5:c.449T>C	ENSP00000419572.1:p.Val150Ala
ENST00000479074.5:n.474T>C
ENST00000479730.5:n.571T>C
ENST00000483041.5:n.585T>C
ENST00000486063.5:n.596T>C
ENST00000488465.1:n.424T>C
NM_000500.7:c.416T>C	NP_000491.4:p.Val139Ala
NM_001128590.3:c.326T>C	NP_001122062.3:p.Val109Ala
XM_011514314.1:c.11T>C	XP_011512616.1:p.Val4Ala
NM_000500.9:c.416T>C MANE Select	NP_000491.4:p.Val139Ala
NM_001368143.1:c.11T>C	NP_001355072.1:p.Val4Ala
NM_001368144.1:c.11T>C	NP_001355073.1:p.Val4Ala
NM_001128590.4:c.326T>C	NP_001122062.3:p.Val109Ala
NM_001368143.2:c.11T>C	NP_001355072.1:p.Val4Ala
NM_001368144.2:c.11T>C	NP_001355073.1:p.Val4Ala