Canonical Allele Identifier: CA2504694728

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040630G>T , CM000668.2:g.32040630G>T	GRCh38
NC_000006.11:g.32008407G>T , CM000668.1:g.32008407G>T	GRCh37
NC_000006.10:g.32116386G>T	NCBI36
NG_007941.2:g.7323G>T
NG_008337.2:g.73745C>A
NG_007941.3:g.7326G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1119-38G>T MANE Select	ENSP00000496625.1:n.1119-38G>T
ENST00000418967.6:c.1119-38G>T	ENSP00000408860.2:n.1119-38G>T
ENST00000435122.3:c.1029-38G>T	ENSP00000415043.2:n.1029-38G>T
ENST00000479074.5:n.1222G>T
ENST00000479730.5:n.1235-38G>T
ENST00000483041.5:n.1288-38G>T
ENST00000486063.5:n.1098-38G>T
NM_000500.7:c.1119-38G>T	NP_000491.4:n.1119-38G>T
NM_001128590.3:c.1029-38G>T	NP_001122062.3:n.1029-38G>T
XM_011514314.1:c.714-38G>T	XP_011512616.1:n.714-38G>T
NM_000500.9:c.1119-38G>T MANE Select	NP_000491.4:n.1119-38G>T
NM_001368143.1:c.714-38G>T	NP_001355072.1:n.714-38G>T
NM_001368144.1:c.714-38G>T	NP_001355073.1:n.714-38G>T
NM_001128590.4:c.1029-38G>T	NP_001122062.3:n.1029-38G>T
NM_001368143.2:c.714-38G>T	NP_001355072.1:n.714-38G>T
NM_001368144.2:c.714-38G>T	NP_001355073.1:n.714-38G>T