Canonical Allele Identifier: CA449819027

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008532A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040755A>C , CM000668.2:g.32040755A>C	GRCh38
NC_000006.11:g.32008532A>C , CM000668.1:g.32008532A>C	GRCh37
NC_000006.10:g.32116511A>C	NCBI36
NG_007941.2:g.7448A>C
NG_008337.2:g.73620T>G
NG_007941.3:g.7451A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1206A>C MANE Select	ENSP00000496625.1:p.Pro402=
ENST00000418967.6:c.1206A>C	ENSP00000408860.2:p.Pro402=
ENST00000435122.3:c.1116A>C	ENSP00000415043.2:p.Pro372=
ENST00000479074.5:n.1347A>C
ENST00000479730.5:n.1322A>C
ENST00000483041.5:n.1375A>C
ENST00000486063.5:n.1185A>C
NM_000500.7:c.1206A>C	NP_000491.4:p.Pro402=
NM_001128590.3:c.1116A>C	NP_001122062.3:p.Pro372=
XM_011514314.1:c.801A>C	XP_011512616.1:p.Pro267=
NM_000500.9:c.1206A>C MANE Select	NP_000491.4:p.Pro402=
NM_001368143.1:c.801A>C	NP_001355072.1:p.Pro267=
NM_001368144.1:c.801A>C	NP_001355073.1:p.Pro267=
NM_001128590.4:c.1116A>C	NP_001122062.3:p.Pro372=
NM_001368143.2:c.801A>C	NP_001355072.1:p.Pro267=
NM_001368144.2:c.801A>C	NP_001355073.1:p.Pro267=