Canonical Allele Identifier: CA363502165

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007021G>C (hg19) ; chr6:g.32039244G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039244G>C , CM000668.2:g.32039244G>C	GRCh38
NC_000006.11:g.32007021G>C , CM000668.1:g.32007021G>C	GRCh37
NC_000006.10:g.32115000G>C	NCBI36
NG_007941.2:g.5937G>C
NG_008337.2:g.75131C>G
NG_007941.3:g.5940G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.443G>C MANE Select	ENSP00000496625.1:p.Cys148Ser
ENST00000418967.6:c.443G>C	ENSP00000408860.2:p.Cys148Ser
ENST00000435122.3:c.353G>C	ENSP00000415043.2:p.Cys118Ser
ENST00000462278.1:n.31G>C
ENST00000464325.5:n.364G>C
ENST00000466779.5:c.*135G>C	ENSP00000417321.1:n.*135G>C
ENST00000466879.5:n.494G>C
ENST00000469053.5:c.*135G>C	ENSP00000418104.1:n.*135G>C
ENST00000471671.4:c.443G>C	ENSP00000418561.1:p.Cys148Ser
ENST00000478281.5:c.476G>C	ENSP00000419572.1:p.Cys159Ser
ENST00000479074.5:n.501G>C
ENST00000479730.5:n.598G>C
ENST00000483041.5:n.612G>C
ENST00000486063.5:n.623G>C
ENST00000488465.1:n.451G>C
NM_000500.7:c.443G>C	NP_000491.4:p.Cys148Ser
NM_001128590.3:c.353G>C	NP_001122062.3:p.Cys118Ser
XM_011514314.1:c.38G>C	XP_011512616.1:p.Cys13Ser
NM_000500.9:c.443G>C MANE Select	NP_000491.4:p.Cys148Ser
NM_001368143.1:c.38G>C	NP_001355072.1:p.Cys13Ser
NM_001368144.1:c.38G>C	NP_001355073.1:p.Cys13Ser
NM_001128590.4:c.353G>C	NP_001122062.3:p.Cys118Ser
NM_001368143.2:c.38G>C	NP_001355072.1:p.Cys13Ser
NM_001368144.2:c.38G>C	NP_001355073.1:p.Cys13Ser