Canonical Allele Identifier: CA2678088253

Gene: CYP21A2

Linked Data

• gnomAD v4: 6-32038399-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038400_32038401del , CM000668.2:g.32038400_32038401del	GRCh38
NC_000006.11:g.32006177_32006178del , CM000668.1:g.32006177_32006178del	GRCh37
NC_000006.10:g.32114156_32114157del	NCBI36
NG_007941.2:g.5096_5097del
NG_007941.3:g.5096_5097del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000418967.6:c.-23_-22del	ENSP00000408860.2:n.-23_-22del
ENST00000466779.5:c.-23_-22del	ENSP00000417321.1:n.-23_-22del
ENST00000478281.5:c.-23_-22del	ENSP00000419572.1:n.-23_-22del
ENST00000479074.5:n.36_37del
ENST00000479730.5:n.36_37del
ENST00000480027.1:n.31_32del
ENST00000483041.5:n.31_32del
ENST00000486063.5:n.61_62del
NM_000500.7:c.-23_-22del	NP_000491.4:n.-23_-22del
NM_001128590.3:c.-23_-22del	NP_001122062.3:n.-23_-22del
XM_011514314.1:c.-447_-446del	XP_011512616.1:n.-447_-446del
NM_001368143.1:c.-447_-446del	NP_001355072.1:n.-447_-446del
NM_001368144.1:c.-357_-356del	NP_001355073.1:n.-357_-356del