Canonical Allele Identifier: CA363500690

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32006873A>C (hg19) ; chr6:g.32039096A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039096A>C , CM000668.2:g.32039096A>C	GRCh38
NC_000006.11:g.32006873A>C , CM000668.1:g.32006873A>C	GRCh37
NC_000006.10:g.32114852A>C	NCBI36
NG_007941.2:g.5789A>C
NG_007941.3:g.5792A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.295A>C MANE Select	ENSP00000496625.1:p.Lys99Gln
ENST00000418967.6:c.295A>C	ENSP00000408860.2:p.Lys99Gln
ENST00000435122.3:c.205A>C	ENSP00000415043.2:p.Lys69Gln
ENST00000464325.5:n.230-14A>C
ENST00000466779.5:c.314A>C	ENSP00000417321.1:p.Gln105Pro
ENST00000466879.5:n.346A>C
ENST00000469053.5:c.224A>C	ENSP00000418104.1:p.Gln75Pro
ENST00000471671.4:c.295A>C	ENSP00000418561.1:p.Lys99Gln
ENST00000478281.5:c.328A>C	ENSP00000419572.1:p.Lys110Gln
ENST00000479074.5:n.353A>C
ENST00000479730.5:n.450A>C
ENST00000480027.1:n.630A>C
ENST00000483041.5:n.464A>C
ENST00000486063.5:n.475A>C
ENST00000488465.1:n.303A>C
NM_000500.7:c.295A>C	NP_000491.4:p.Lys99Gln
NM_001128590.3:c.205A>C	NP_001122062.3:p.Lys69Gln
XM_011514314.1:c.-111A>C	XP_011512616.1:n.-111A>C
NM_000500.9:c.295A>C MANE Select	NP_000491.4:p.Lys99Gln
NM_001368143.1:c.-111A>C	NP_001355072.1:n.-111A>C
NM_001368144.1:c.-111A>C	NP_001355073.1:n.-111A>C
NM_001128590.4:c.205A>C	NP_001122062.3:p.Lys69Gln
NM_001368143.2:c.-111A>C	NP_001355072.1:n.-111A>C
NM_001368144.2:c.-111A>C	NP_001355073.1:n.-111A>C