Canonical Allele Identifier: CA2678088629

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32039023-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039025del , CM000668.2:g.32039025del	GRCh38
NC_000006.11:g.32006802del , CM000668.1:g.32006802del	GRCh37
NC_000006.10:g.32114781del	NCBI36
NG_007941.2:g.5718del
NG_007941.3:g.5721del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.293-69del MANE Select	ENSP00000496625.1:n.293-69del
ENST00000418967.6:c.293-69del	ENSP00000408860.2:n.293-69del
ENST00000435122.3:c.203-69del	ENSP00000415043.2:n.203-69del
ENST00000464325.5:n.230-85del
ENST00000466779.5:c.293-50del	ENSP00000417321.1:n.293-50del
ENST00000466879.5:n.275del
ENST00000469053.5:c.203-50del	ENSP00000418104.1:n.203-50del
ENST00000471671.4:c.293-69del	ENSP00000418561.1:n.293-69del
ENST00000478281.5:c.293-36del	ENSP00000419572.1:n.293-36del
ENST00000479074.5:n.351-69del
ENST00000479730.5:n.448-69del
ENST00000480027.1:n.559del
ENST00000483041.5:n.443-50del
ENST00000486063.5:n.473-69del
ENST00000488465.1:n.301-69del
NM_000500.7:c.293-69del	NP_000491.4:n.293-69del
NM_001128590.3:c.203-69del	NP_001122062.3:n.203-69del
XM_011514314.1:c.-132-50del	XP_011512616.1:n.-132-50del
NM_000500.9:c.293-69del MANE Select	NP_000491.4:n.293-69del
NM_001368143.1:c.-132-50del	NP_001355072.1:n.-132-50del
NM_001368144.1:c.-132-50del	NP_001355073.1:n.-132-50del
NM_001128590.4:c.203-69del	NP_001122062.3:n.203-69del
NM_001368143.2:c.-132-50del	NP_001355072.1:n.-132-50del
NM_001368144.2:c.-132-50del	NP_001355073.1:n.-132-50del