Canonical Allele Identifier: CA363506620

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007856A>C (hg19) ; chr6:g.32040079A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040079A>C , CM000668.2:g.32040079A>C	GRCh38
NC_000006.11:g.32007856A>C , CM000668.1:g.32007856A>C	GRCh37
NC_000006.10:g.32115835A>C	NCBI36
NG_007941.2:g.6772A>C
NG_008337.2:g.74296T>G
NG_007941.3:g.6775A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.813A>C MANE Select	ENSP00000496625.1:p.Glu271Asp
ENST00000418967.6:c.813A>C	ENSP00000408860.2:p.Glu271Asp
ENST00000435122.3:c.723A>C	ENSP00000415043.2:p.Glu241Asp
ENST00000479074.5:n.871A>C
ENST00000479730.5:n.929A>C
ENST00000483041.5:n.982A>C
ENST00000486063.5:n.918+244A>C
NM_000500.7:c.813A>C	NP_000491.4:p.Glu271Asp
NM_001128590.3:c.723A>C	NP_001122062.3:p.Glu241Asp
XM_011514314.1:c.408A>C	XP_011512616.1:p.Glu136Asp
NM_000500.9:c.813A>C MANE Select	NP_000491.4:p.Glu271Asp
NM_001368143.1:c.408A>C	NP_001355072.1:p.Glu136Asp
NM_001368144.1:c.408A>C	NP_001355073.1:p.Glu136Asp
NM_001128590.4:c.723A>C	NP_001122062.3:p.Glu241Asp
NM_001368143.2:c.408A>C	NP_001355072.1:p.Glu136Asp
NM_001368144.2:c.408A>C	NP_001355073.1:p.Glu136Asp