Canonical Allele Identifier: CA363510579

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008207C>A (hg19) ; chr6:g.32040430C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040430C>A , CM000668.2:g.32040430C>A	GRCh38
NC_000006.11:g.32008207C>A , CM000668.1:g.32008207C>A	GRCh37
NC_000006.10:g.32116186C>A	NCBI36
NG_007941.2:g.7123C>A
NG_008337.2:g.73945G>T
NG_007941.3:g.7126C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.964C>A MANE Select	ENSP00000496625.1:p.Leu322Ile
ENST00000418967.6:c.964C>A	ENSP00000408860.2:p.Leu322Ile
ENST00000435122.3:c.874C>A	ENSP00000415043.2:p.Leu292Ile
ENST00000479074.5:n.1022C>A
ENST00000479730.5:n.1080C>A
ENST00000483041.5:n.1133C>A
ENST00000486063.5:n.943C>A
NM_000500.7:c.964C>A	NP_000491.4:p.Leu322Ile
NM_001128590.3:c.874C>A	NP_001122062.3:p.Leu292Ile
XM_011514314.1:c.559C>A	XP_011512616.1:p.Leu187Ile
NM_000500.9:c.964C>A MANE Select	NP_000491.4:p.Leu322Ile
NM_001368143.1:c.559C>A	NP_001355072.1:p.Leu187Ile
NM_001368144.1:c.559C>A	NP_001355073.1:p.Leu187Ile
NM_001128590.4:c.874C>A	NP_001122062.3:p.Leu292Ile
NM_001368143.2:c.559C>A	NP_001355072.1:p.Leu187Ile
NM_001368144.2:c.559C>A	NP_001355073.1:p.Leu187Ile