Canonical Allele Identifier: CA363510960

Gene: CYP21A2

Linked Data

• MyVariant Identifiers: chr6:g.32008264G>A (hg19) ; chr6:g.32040487G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32040487G>A , CM000668.2:g.32040487G>A	GRCh38
NC_000006.11:g.32008264G>A , CM000668.1:g.32008264G>A	GRCh37
NC_000006.10:g.32116243G>A	NCBI36
NG_007941.2:g.7180G>A
NG_008337.2:g.73888C>T
NG_007941.3:g.7183G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000644719.2:c.1021G>A MANE Select	ENSP00000496625.1:p.Ala341Thr
ENST00000418967.6:c.1021G>A	ENSP00000408860.2:p.Ala341Thr
ENST00000435122.3:c.931G>A	ENSP00000415043.2:p.Ala311Thr
ENST00000479074.5:n.1079G>A
ENST00000479730.5:n.1137G>A
ENST00000483041.5:n.1190G>A
ENST00000486063.5:n.1000G>A
NM_000500.7:c.1021G>A	NP_000491.4:p.Ala341Thr
NM_001128590.3:c.931G>A	NP_001122062.3:p.Ala311Thr
XM_011514314.1:c.616G>A	XP_011512616.1:p.Ala206Thr
NM_000500.9:c.1021G>A MANE Select	NP_000491.4:p.Ala341Thr
NM_001368143.1:c.616G>A	NP_001355072.1:p.Ala206Thr
NM_001368144.1:c.616G>A	NP_001355073.1:p.Ala206Thr
NM_001128590.4:c.931G>A	NP_001122062.3:p.Ala311Thr
NM_001368143.2:c.616G>A	NP_001355072.1:p.Ala206Thr
NM_001368144.2:c.616G>A	NP_001355073.1:p.Ala206Thr