Canonical Allele Identifier: CA1619396402

Gene: CYP21A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32038526_32038527delinsCG , CM000668.2:g.32038526_32038527delinsCG	GRCh38
NC_000006.11:g.32006303_32006304delinsCG , CM000668.1:g.32006303_32006304delinsCG	GRCh37
NC_000006.10:g.32114282_32114283delinsCG	NCBI36
NG_007941.2:g.5219_5220delinsCG
NG_007941.3:g.5222_5223delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.104_105delinsCG MANE Select	ENSP00000496625.1:p.Pro35=
ENST00000418967.6:c.104_105delinsCG	ENSP00000408860.2:p.Pro35=
ENST00000435122.3:c.104_105delinsCG	ENSP00000415043.2:p.Pro35=
ENST00000466779.5:c.104_105delinsCG	ENSP00000417321.1:p.Pro35=
ENST00000469053.5:c.104_105delinsCG	ENSP00000418104.1:p.Pro35=
ENST00000471671.4:c.104_105delinsCG	ENSP00000418561.1:p.Pro35=
ENST00000478281.5:c.104_105delinsCG	ENSP00000419572.1:p.Pro35=
ENST00000479074.5:n.162_163delinsCG
ENST00000479730.5:n.162_163delinsCG
ENST00000480027.1:n.157_158delinsCG
ENST00000483041.5:n.157_158delinsCG
ENST00000486063.5:n.187_188delinsCG
ENST00000488465.1:n.112_113delinsCG
NM_000500.7:c.104_105delinsCG	NP_000491.4:p.Pro35=
NM_001128590.3:c.104_105delinsCG	NP_001122062.3:p.Pro35=
XM_011514314.1:c.-321_-320delinsCG	XP_011512616.1:n.-321_-320delinsCG
NM_000500.9:c.104_105delinsCG MANE Select	NP_000491.4:p.Pro35=
NM_001368143.1:c.-321_-320delinsCG	NP_001355072.1:n.-321_-320delinsCG
NM_001368144.1:c.-231_-230delinsCG	NP_001355073.1:n.-231_-230delinsCG
NM_001128590.4:c.104_105delinsCG	NP_001122062.3:p.Pro35=
NM_001368143.2:c.-321_-320delinsCG	NP_001355072.1:n.-321_-320delinsCG
NM_001368144.2:c.-231_-230delinsCG	NP_001355073.1:n.-231_-230delinsCG