Canonical Allele Identifier: CA2176791166

Gene: CYP19A1 PIRC66 MIR4713HG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51287420C= , CM000677.2:g.51287420C=	GRCh38
NC_000015.9:g.51579617C= , CM000677.1:g.51579617C=	GRCh37
NC_000015.8:g.49366909C=	NCBI36
NG_007982.1:g.56179G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396402.6:c.-38-44470G= (CYP19A1) MANE Select	ENSP00000379683.1:n.-38-44470G=
ENST00000260433.6:c.-39+36396G= (CYP19A1)	ENSP00000260433.2:n.-39+36396G=
ENST00000396402.5:c.-38-44470G= (CYP19A1)	ENSP00000379683.1:n.-38-44470G=
ENST00000396404.8:c.-39+36396G= (CYP19A1)	ENSP00000379685.4:n.-39+36396G=
ENST00000405011.6:c.-193-9258G= (CYP19A1)	ENSP00000384389.2:n.-193-9258G=
ENST00000439712.6:c.-282-31659G= (CYP19A1)	ENSP00000390614.2:n.-282-31659G=
ENST00000453807.6:c.-229-31712G= (CYP19A1)	ENSP00000391139.2:n.-229-31712G=
ENST00000557858.5:c.-38-44470G= (CYP19A1)	ENSP00000452627.1:n.-38-44470G=
ENST00000557934.5:c.-38-44470G= (CYP19A1)	ENSP00000454004.1:n.-38-44470G=
ENST00000558328.5:c.-38-44470G= (CYP19A1)	ENSP00000453280.1:n.-38-44470G=
ENST00000559646.1:c.-39+31013G= (CYP19A1)	ENSP00000453318.1:n.-39+31013G=
ENST00000559980.5:c.-282-31659G= (CYP19A1)	ENSP00000452872.1:n.-282-31659G=
ENST00000561075.5:c.-38-44470G= (CYP19A1)	ENSP00000454039.1:n.-38-44470G=
NM_000103.3:c.-38-44470G= (CYP19A1)	NP_000094.2:n.-38-44470G=
NM_031226.2:c.-39+36396G= (CYP19A1)	NP_112503.1:n.-39+36396G=
XM_005254191.1:c.-39+31013G= (CYP19A1)	XP_005254248.1:n.-39+31013G=
XR_932221.1:n.5385+6113C= (PIRC66)
NM_001347248.1:c.-39+36396G= (CYP19A1)	NP_001334177.1:n.-39+36396G=
NM_001347249.1:c.-39+31013G= (CYP19A1)	NP_001334178.1:n.-39+31013G=
NM_001347250.1:c.-39+830G= (CYP19A1)	NP_001334179.1:n.-39+830G=
NR_146310.1:n.263-6194C= (MIR4713HG)
NM_000103.4:c.-38-44470G= (CYP19A1) MANE Select	NP_000094.2:n.-38-44470G=
NM_001347249.2:c.-39+31013G= (CYP19A1)	NP_001334178.1:n.-39+31013G=
NM_031226.3:c.-39+36396G= (CYP19A1)	NP_112503.1:n.-39+36396G=
NM_001347250.2:c.-39+830G= (CYP19A1)	NP_001334179.1:n.-39+830G=