Canonical Allele Identifier: CA2770519741

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040365T>C , CM000668.2:g.32040365T>C	GRCh38
NC_000006.11:g.32008142T>C , CM000668.1:g.32008142T>C	GRCh37
NC_000006.10:g.32116121T>C	NCBI36
NG_007941.2:g.7058T>C
NG_008337.2:g.74010A>G
NG_007941.3:g.7061T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.940-41T>C MANE Select	ENSP00000496625.1:n.940-41T>C
ENST00000418967.6:c.940-41T>C	ENSP00000408860.2:n.940-41T>C
ENST00000435122.3:c.850-41T>C	ENSP00000415043.2:n.850-41T>C
ENST00000479074.5:n.998-41T>C
ENST00000479730.5:n.1056-41T>C
ENST00000483041.5:n.1109-41T>C
ENST00000486063.5:n.919-41T>C
NM_000500.7:c.940-41T>C	NP_000491.4:n.940-41T>C
NM_001128590.3:c.850-41T>C	NP_001122062.3:n.850-41T>C
XM_011514314.1:c.535-41T>C	XP_011512616.1:n.535-41T>C
NM_000500.9:c.940-41T>C MANE Select	NP_000491.4:n.940-41T>C
NM_001368143.1:c.535-41T>C	NP_001355072.1:n.535-41T>C
NM_001368144.1:c.535-41T>C	NP_001355073.1:n.535-41T>C
NM_001128590.4:c.850-41T>C	NP_001122062.3:n.850-41T>C
NM_001368143.2:c.535-41T>C	NP_001355072.1:n.535-41T>C
NM_001368144.2:c.535-41T>C	NP_001355073.1:n.535-41T>C