Canonical Allele Identifier: CA2176800898

Gene: CYP19A1 PIRC66

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51302783C= , CM000677.2:g.51302783C=	GRCh38
NC_000015.9:g.51594980C= , CM000677.1:g.51594980C=	GRCh37
NC_000015.8:g.49382272C=	NCBI36
NG_007982.1:g.40816G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000396402.6:c.-39+35712G= (CYP19A1) MANE Select	ENSP00000379683.1:n.-39+35712G=
ENST00000260433.6:c.-39+21033G= (CYP19A1)	ENSP00000260433.2:n.-39+21033G=
ENST00000396402.5:c.-39+35712G= (CYP19A1)	ENSP00000379683.1:n.-39+35712G=
ENST00000396404.8:c.-39+21033G= (CYP19A1)	ENSP00000379685.4:n.-39+21033G=
ENST00000405011.6:c.-193-24621G= (CYP19A1)	ENSP00000384389.2:n.-193-24621G=
ENST00000439712.6:c.-283+35712G= (CYP19A1)	ENSP00000390614.2:n.-283+35712G=
ENST00000453807.6:c.-230+35712G= (CYP19A1)	ENSP00000391139.2:n.-230+35712G=
ENST00000557858.5:c.-39+35712G= (CYP19A1)	ENSP00000452627.1:n.-39+35712G=
ENST00000557934.5:c.-39+35712G= (CYP19A1)	ENSP00000454004.1:n.-39+35712G=
ENST00000558328.5:c.-39+35654G= (CYP19A1)	ENSP00000453280.1:n.-39+35654G=
ENST00000559646.1:c.-39+15650G= (CYP19A1)	ENSP00000453318.1:n.-39+15650G=
ENST00000559980.5:c.-283+35035G= (CYP19A1)	ENSP00000452872.1:n.-283+35035G=
ENST00000561075.5:c.-39+35712G= (CYP19A1)	ENSP00000454039.1:n.-39+35712G=
NM_000103.3:c.-39+35712G= (CYP19A1)	NP_000094.2:n.-39+35712G=
NM_031226.2:c.-39+21033G= (CYP19A1)	NP_112503.1:n.-39+21033G=
XM_005254191.1:c.-39+15650G= (CYP19A1)	XP_005254248.1:n.-39+15650G=
XR_932223.1:n.5108C= (PIRC66)
XR_932229.1:n.5108C= (PIRC66)
NM_001347248.1:c.-39+21033G= (CYP19A1)	NP_001334177.1:n.-39+21033G=
NM_001347249.1:c.-39+15650G= (CYP19A1)	NP_001334178.1:n.-39+15650G=
NM_000103.4:c.-39+35712G= (CYP19A1) MANE Select	NP_000094.2:n.-39+35712G=
NM_001347249.2:c.-39+15650G= (CYP19A1)	NP_001334178.1:n.-39+15650G=
NM_031226.3:c.-39+21033G= (CYP19A1)	NP_112503.1:n.-39+21033G=