Canonical Allele Identifier: CA2176809022

Gene: CYP19A1 PIRC66

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51321307A= , CM000677.2:g.51321307A=	GRCh38
NC_000015.9:g.51613504A= , CM000677.1:g.51613504A=	GRCh37
NC_000015.8:g.49400796A=	NCBI36
NG_007982.1:g.22292T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396402.6:c.-39+17188T= (CYP19A1) MANE Select	ENSP00000379683.1:n.-39+17188T=
ENST00000260433.6:c.-39+2509T= (CYP19A1)	ENSP00000260433.2:n.-39+2509T=
ENST00000396402.5:c.-39+17188T= (CYP19A1)	ENSP00000379683.1:n.-39+17188T=
ENST00000396404.8:c.-39+2509T= (CYP19A1)	ENSP00000379685.4:n.-39+2509T=
ENST00000405011.6:c.-194+17188T= (CYP19A1)	ENSP00000384389.2:n.-194+17188T=
ENST00000439712.6:c.-283+17188T= (CYP19A1)	ENSP00000390614.2:n.-283+17188T=
ENST00000453807.6:c.-230+17188T= (CYP19A1)	ENSP00000391139.2:n.-230+17188T=
ENST00000492852.1:n.88-934T= (CYP19A1)
ENST00000557858.5:c.-39+17188T= (CYP19A1)	ENSP00000452627.1:n.-39+17188T=
ENST00000557934.5:c.-39+17188T= (CYP19A1)	ENSP00000454004.1:n.-39+17188T=
ENST00000558328.5:c.-39+17130T= (CYP19A1)	ENSP00000453280.1:n.-39+17130T=
ENST00000559980.5:c.-283+16511T= (CYP19A1)	ENSP00000452872.1:n.-283+16511T=
ENST00000561075.5:c.-39+17188T= (CYP19A1)	ENSP00000454039.1:n.-39+17188T=
NM_000103.3:c.-39+17188T= (CYP19A1)	NP_000094.2:n.-39+17188T=
NM_031226.2:c.-39+2509T= (CYP19A1)	NP_112503.1:n.-39+2509T=
XR_932224.1:n.3308+268A= (PIRC66)
XR_932226.1:n.2601+268A= (PIRC66)
XR_932229.1:n.6085+268A= (PIRC66)
XR_932230.1:n.384+268A= (PIRC66)
NM_001347248.1:c.-39+2509T= (CYP19A1)	NP_001334177.1:n.-39+2509T=
XR_002957708.1:n.364+268A=
NM_000103.4:c.-39+17188T= (CYP19A1) MANE Select	NP_000094.2:n.-39+17188T=
NM_031226.3:c.-39+2509T= (CYP19A1)	NP_112503.1:n.-39+2509T=