Canonical Allele Identifier: CA449729073

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32007013G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039236G>A , CM000668.2:g.32039236G>A	GRCh38
NC_000006.11:g.32007013G>A , CM000668.1:g.32007013G>A	GRCh37
NC_000006.10:g.32114992G>A	NCBI36
NG_007941.2:g.5929G>A
NG_008337.2:g.75139C>T
NG_007941.3:g.5932G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.435G>A MANE Select	ENSP00000496625.1:p.Gln145=
ENST00000418967.6:c.435G>A	ENSP00000408860.2:p.Gln145=
ENST00000435122.3:c.345G>A	ENSP00000415043.2:p.Gln115=
ENST00000462278.1:n.23G>A
ENST00000464325.5:n.356G>A
ENST00000466779.5:c.*127G>A	ENSP00000417321.1:n.*127G>A
ENST00000466879.5:n.486G>A
ENST00000469053.5:c.*127G>A	ENSP00000418104.1:n.*127G>A
ENST00000471671.4:c.435G>A	ENSP00000418561.1:p.Gln145=
ENST00000478281.5:c.468G>A	ENSP00000419572.1:p.Gln156=
ENST00000479074.5:n.493G>A
ENST00000479730.5:n.590G>A
ENST00000483041.5:n.604G>A
ENST00000486063.5:n.615G>A
ENST00000488465.1:n.443G>A
NM_000500.7:c.435G>A	NP_000491.4:p.Gln145=
NM_001128590.3:c.345G>A	NP_001122062.3:p.Gln115=
XM_011514314.1:c.30G>A	XP_011512616.1:p.Gln10=
NM_000500.9:c.435G>A MANE Select	NP_000491.4:p.Gln145=
NM_001368143.1:c.30G>A	NP_001355072.1:p.Gln10=
NM_001368144.1:c.30G>A	NP_001355073.1:p.Gln10=
NM_001128590.4:c.345G>A	NP_001122062.3:p.Gln115=
NM_001368143.2:c.30G>A	NP_001355072.1:p.Gln10=
NM_001368144.2:c.30G>A	NP_001355073.1:p.Gln10=