Canonical Allele Identifier: CA650916185

Gene: CYP21A2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039081_32039082insA , CM000668.2:g.32039081_32039082insA	GRCh38
NC_000006.11:g.32006858_32006859insA , CM000668.1:g.32006858_32006859insA	GRCh37
NC_000006.10:g.32114837_32114838insA	NCBI36
NG_007941.2:g.5774_5775insA
NG_007941.3:g.5777_5778insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.293-13_293-12insA MANE Select	ENSP00000496625.1:n.293-13_293-12insA
ENST00000418967.6:c.293-13_293-12insA	ENSP00000408860.2:n.293-13_293-12insA
ENST00000435122.3:c.203-13_203-12insA	ENSP00000415043.2:n.203-13_203-12insA
ENST00000464325.5:n.230-29_230-28insA
ENST00000466779.5:c.299_300insA	ENSP00000417321.1:p.Ser101LeufsTer?
ENST00000466879.5:n.331_332insA
ENST00000469053.5:c.209_210insA	ENSP00000418104.1:p.Ser71LeufsTer?
ENST00000471671.4:c.293-13_293-12insA	ENSP00000418561.1:n.293-13_293-12insA
ENST00000478281.5:c.313_314insA	ENSP00000419572.1:p.Pro105HisfsTer10
ENST00000479074.5:n.351-13_351-12insA
ENST00000479730.5:n.448-13_448-12insA
ENST00000480027.1:n.615_616insA
ENST00000483041.5:n.449_450insA
ENST00000486063.5:n.473-13_473-12insA
ENST00000488465.1:n.301-13_301-12insA
NM_000500.7:c.293-13_293-12insA	NP_000491.4:n.293-13_293-12insA
NM_001128590.3:c.203-13_203-12insA	NP_001122062.3:n.203-13_203-12insA
XM_011514314.1:c.-126_-125insA	XP_011512616.1:n.-126_-125insA
NM_000500.9:c.293-13_293-12insA MANE Select	NP_000491.4:n.293-13_293-12insA
NM_001368143.1:c.-126_-125insA	NP_001355072.1:n.-126_-125insA
NM_001368144.1:c.-126_-125insA	NP_001355073.1:n.-126_-125insA
NM_001128590.4:c.203-13_203-12insA	NP_001122062.3:n.203-13_203-12insA
NM_001368143.2:c.-126_-125insA	NP_001355072.1:n.-126_-125insA
NM_001368144.2:c.-126_-125insA	NP_001355073.1:n.-126_-125insA