Canonical Allele Identifier: CA1087498398

Gene: CYP21A2

Linked Data

• dbSNP Id: rs1776041625
• gnomAD v3: 6-32039007-A-AAG
• gnomAD v4: 6-32039007-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039008_32039009insGA , CM000668.2:g.32039008_32039009insGA	GRCh38
NC_000006.11:g.32006785_32006786insGA , CM000668.1:g.32006785_32006786insGA	GRCh37
NC_000006.10:g.32114764_32114765insGA	NCBI36
NG_007941.2:g.5701_5702insGA
NG_007941.3:g.5704_5705insGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.293-86_293-85insGA MANE Select	ENSP00000496625.1:n.293-86_293-85insGA
ENST00000418967.6:c.293-86_293-85insGA	ENSP00000408860.2:n.293-86_293-85insGA
ENST00000435122.3:c.203-86_203-85insGA	ENSP00000415043.2:n.203-86_203-85insGA
ENST00000464325.5:n.230-102_230-101insGA
ENST00000466779.5:c.293-67_293-66insGA	ENSP00000417321.1:n.293-67_293-66insGA
ENST00000466879.5:n.258_259insGA
ENST00000469053.5:c.203-67_203-66insGA	ENSP00000418104.1:n.203-67_203-66insGA
ENST00000471671.4:c.293-86_293-85insGA	ENSP00000418561.1:n.293-86_293-85insGA
ENST00000478281.5:c.293-53_293-52insGA	ENSP00000419572.1:n.293-53_293-52insGA
ENST00000479074.5:n.351-86_351-85insGA
ENST00000479730.5:n.448-86_448-85insGA
ENST00000480027.1:n.542_543insGA
ENST00000483041.5:n.443-67_443-66insGA
ENST00000486063.5:n.473-86_473-85insGA
ENST00000488465.1:n.301-86_301-85insGA
NM_000500.7:c.293-86_293-85insGA	NP_000491.4:n.293-86_293-85insGA
NM_001128590.3:c.203-86_203-85insGA	NP_001122062.3:n.203-86_203-85insGA
XM_011514314.1:c.-132-67_-132-66insGA	XP_011512616.1:n.-132-67_-132-66insGA
NM_000500.9:c.293-86_293-85insGA MANE Select	NP_000491.4:n.293-86_293-85insGA
NM_001368143.1:c.-132-67_-132-66insGA	NP_001355072.1:n.-132-67_-132-66insGA
NM_001368144.1:c.-132-67_-132-66insGA	NP_001355073.1:n.-132-67_-132-66insGA
NM_001128590.4:c.203-86_203-85insGA	NP_001122062.3:n.203-86_203-85insGA
NM_001368143.2:c.-132-67_-132-66insGA	NP_001355072.1:n.-132-67_-132-66insGA
NM_001368144.2:c.-132-67_-132-66insGA	NP_001355073.1:n.-132-67_-132-66insGA