Canonical Allele Identifier: CA392421124

Gene: CYP19A1 PIRC66 MIR4713HG

Linked Data

• MyVariant Identifiers: chr15:g.51520021T>A (hg19) ; chr15:g.51227824T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51227824T>A , CM000677.2:g.51227824T>A	GRCh38
NC_000015.9:g.51520021T>A , CM000677.1:g.51520021T>A	GRCh37
NC_000015.8:g.49307313T>A	NCBI36
NG_007982.1:g.115775A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396402.6:c.406A>T (CYP19A1) MANE Select	ENSP00000379683.1:p.Asn136Tyr
ENST00000260433.6:c.406A>T (CYP19A1)	ENSP00000260433.2:p.Asn136Tyr
ENST00000396402.5:c.406A>T (CYP19A1)	ENSP00000379683.1:p.Asn136Tyr
ENST00000396404.8:c.406A>T (CYP19A1)	ENSP00000379685.4:p.Asn136Tyr
ENST00000405011.6:c.406A>T (CYP19A1)	ENSP00000384389.2:p.Asn136Tyr
ENST00000405913.7:c.406A>T (CYP19A1)	ENSP00000383930.3:p.Asn136Tyr
ENST00000439712.6:c.406A>T (CYP19A1)	ENSP00000390614.2:p.Asn136Tyr
ENST00000453807.6:c.406A>T (CYP19A1)	ENSP00000391139.2:p.Asn136Tyr
ENST00000557858.5:c.406A>T (CYP19A1)	ENSP00000452627.1:p.Asn136Tyr
ENST00000557934.5:c.406A>T (CYP19A1)	ENSP00000454004.1:p.Asn136Tyr
ENST00000558328.5:c.406A>T (CYP19A1)	ENSP00000453280.1:p.Asn136Tyr
ENST00000559646.1:c.406A>T (CYP19A1)	ENSP00000453318.1:p.Asn136Tyr
ENST00000559878.5:c.406A>T (CYP19A1)	ENSP00000453149.1:p.Asn136Tyr
ENST00000559980.5:c.406A>T (CYP19A1)	ENSP00000452872.1:p.Asn136Tyr
ENST00000561075.5:c.406A>T (CYP19A1)	ENSP00000454039.1:p.Asn136Tyr
NM_000103.3:c.406A>T (CYP19A1)	NP_000094.2:p.Asn136Tyr
NM_031226.2:c.406A>T (CYP19A1)	NP_112503.1:p.Asn136Tyr
XM_005254190.1:c.406A>T (CYP19A1)	XP_005254247.1:p.Asn136Tyr
XM_005254191.1:c.406A>T (CYP19A1)	XP_005254248.1:p.Asn136Tyr
XR_932222.1:n.99-50159T>A (PIRC66)
NM_001347248.1:c.406A>T (CYP19A1)	NP_001334177.1:p.Asn136Tyr
NM_001347249.1:c.406A>T (CYP19A1)	NP_001334178.1:p.Asn136Tyr
NM_001347250.1:c.406A>T (CYP19A1)	NP_001334179.1:p.Asn136Tyr
NM_001347251.1:c.406A>T (CYP19A1)	NP_001334180.1:p.Asn136Tyr
NM_001347252.1:c.406A>T (CYP19A1)	NP_001334181.1:p.Asn136Tyr
NM_001347253.1:c.406A>T (CYP19A1)	NP_001334182.1:p.Asn136Tyr
NM_001347254.1:c.406A>T (CYP19A1)	NP_001334183.1:p.Asn136Tyr
NM_001347255.1:c.406A>T (CYP19A1)	NP_001334184.1:p.Asn136Tyr
NM_001347256.1:c.406A>T (CYP19A1)	NP_001334185.1:p.Asn136Tyr
NR_146310.1:n.195-50159T>A (MIR4713HG)
NM_000103.4:c.406A>T (CYP19A1) MANE Select	NP_000094.2:p.Asn136Tyr
NM_001347249.2:c.406A>T (CYP19A1)	NP_001334178.1:p.Asn136Tyr
NM_001347255.2:c.406A>T (CYP19A1)	NP_001334184.1:p.Asn136Tyr
NM_001347256.2:c.406A>T (CYP19A1)	NP_001334185.1:p.Asn136Tyr
NM_031226.3:c.406A>T (CYP19A1)	NP_112503.1:p.Asn136Tyr
NM_001347250.2:c.406A>T (CYP19A1)	NP_001334179.1:p.Asn136Tyr
NM_001347251.2:c.406A>T (CYP19A1)	NP_001334180.1:p.Asn136Tyr
NM_001347252.2:c.406A>T (CYP19A1)	NP_001334181.1:p.Asn136Tyr
NM_001347253.2:c.406A>T (CYP19A1)	NP_001334182.1:p.Asn136Tyr
NM_001347254.2:c.406A>T (CYP19A1)	NP_001334183.1:p.Asn136Tyr