Canonical Allele Identifier: CA1619397144

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32039758A= , CM000668.2:g.32039758A=	GRCh38
NC_000006.11:g.32007535A= , CM000668.1:g.32007535A=	GRCh37
NC_000006.10:g.32115514A=	NCBI36
NG_007941.2:g.6451A=
NG_008337.2:g.74617T=
NG_007941.3:g.6454A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644719.2:c.661A= MANE Select	ENSP00000496625.1:p.Asn221=
ENST00000418967.6:c.661A=	ENSP00000408860.2:p.Asn221=
ENST00000435122.3:c.571A=	ENSP00000415043.2:p.Asn191=
ENST00000462278.1:n.350A=
ENST00000466779.5:c.*353A=	ENSP00000417321.1:n.*353A=
ENST00000466879.5:n.712A=
ENST00000479074.5:n.719A=
ENST00000479730.5:n.777A=
ENST00000483041.5:n.830A=
ENST00000486063.5:n.841A=
NM_000500.7:c.661A=	NP_000491.4:p.Asn221=
NM_001128590.3:c.571A=	NP_001122062.3:p.Asn191=
XM_011514314.1:c.256A=	XP_011512616.1:p.Asn86=
NM_000500.9:c.661A= MANE Select	NP_000491.4:p.Asn221=
NM_001368143.1:c.256A=	NP_001355072.1:p.Asn86=
NM_001368144.1:c.256A=	NP_001355073.1:p.Asn86=
NM_001128590.4:c.571A=	NP_001122062.3:p.Asn191=
NM_001368143.2:c.256A=	NP_001355072.1:p.Asn86=
NM_001368144.2:c.256A=	NP_001355073.1:p.Asn86=