Canonical Allele Identifier: CA490363699

Gene: CYP19A1 PIRC66

Linked Data

• MyVariant Identifiers: chr15:g.51613820T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51321623T>A , CM000677.2:g.51321623T>A	GRCh38
NC_000015.9:g.51613820T>A , CM000677.1:g.51613820T>A	GRCh37
NC_000015.8:g.49401112T>A	NCBI36
NG_007982.1:g.21976A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396402.6:c.-39+16872A>T (CYP19A1) MANE Select	ENSP00000379683.1:n.-39+16872A>T
ENST00000260433.6:c.-39+2193A>T (CYP19A1)	ENSP00000260433.2:n.-39+2193A>T
ENST00000396402.5:c.-39+16872A>T (CYP19A1)	ENSP00000379683.1:n.-39+16872A>T
ENST00000396404.8:c.-39+2193A>T (CYP19A1)	ENSP00000379685.4:n.-39+2193A>T
ENST00000405011.6:c.-194+16872A>T (CYP19A1)	ENSP00000384389.2:n.-194+16872A>T
ENST00000439712.6:c.-283+16872A>T (CYP19A1)	ENSP00000390614.2:n.-283+16872A>T
ENST00000453807.6:c.-230+16872A>T (CYP19A1)	ENSP00000391139.2:n.-230+16872A>T
ENST00000492852.1:n.88-1250A>T (CYP19A1)
ENST00000557858.5:c.-39+16872A>T (CYP19A1)	ENSP00000452627.1:n.-39+16872A>T
ENST00000557934.5:c.-39+16872A>T (CYP19A1)	ENSP00000454004.1:n.-39+16872A>T
ENST00000558328.5:c.-39+16814A>T (CYP19A1)	ENSP00000453280.1:n.-39+16814A>T
ENST00000559980.5:c.-283+16195A>T (CYP19A1)	ENSP00000452872.1:n.-283+16195A>T
ENST00000561075.5:c.-39+16872A>T (CYP19A1)	ENSP00000454039.1:n.-39+16872A>T
NM_000103.3:c.-39+16872A>T (CYP19A1)	NP_000094.2:n.-39+16872A>T
NM_031226.2:c.-39+2193A>T (CYP19A1)	NP_112503.1:n.-39+2193A>T
XR_932224.1:n.3323T>A (PIRC66)
XR_932226.1:n.2616T>A (PIRC66)
XR_932229.1:n.6100T>A (PIRC66)
XR_932230.1:n.399T>A (PIRC66)
NM_001347248.1:c.-39+2193A>T (CYP19A1)	NP_001334177.1:n.-39+2193A>T
XR_002957708.1:n.379T>A
NM_000103.4:c.-39+16872A>T (CYP19A1) MANE Select	NP_000094.2:n.-39+16872A>T
NM_031226.3:c.-39+2193A>T (CYP19A1)	NP_112503.1:n.-39+2193A>T