Canonical Allele Identifier: CA490363697

Gene: CYP19A1 PIRC66

Linked Data

• gnomAD v4: 15-51321622-G-T
• MyVariant Identifiers: chr15:g.51613819G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51321622G>T , CM000677.2:g.51321622G>T	GRCh38
NC_000015.9:g.51613819G>T , CM000677.1:g.51613819G>T	GRCh37
NC_000015.8:g.49401111G>T	NCBI36
NG_007982.1:g.21977C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396402.6:c.-39+16873C>A (CYP19A1) MANE Select	ENSP00000379683.1:n.-39+16873C>A
ENST00000260433.6:c.-39+2194C>A (CYP19A1)	ENSP00000260433.2:n.-39+2194C>A
ENST00000396402.5:c.-39+16873C>A (CYP19A1)	ENSP00000379683.1:n.-39+16873C>A
ENST00000396404.8:c.-39+2194C>A (CYP19A1)	ENSP00000379685.4:n.-39+2194C>A
ENST00000405011.6:c.-194+16873C>A (CYP19A1)	ENSP00000384389.2:n.-194+16873C>A
ENST00000439712.6:c.-283+16873C>A (CYP19A1)	ENSP00000390614.2:n.-283+16873C>A
ENST00000453807.6:c.-230+16873C>A (CYP19A1)	ENSP00000391139.2:n.-230+16873C>A
ENST00000492852.1:n.88-1249C>A (CYP19A1)
ENST00000557858.5:c.-39+16873C>A (CYP19A1)	ENSP00000452627.1:n.-39+16873C>A
ENST00000557934.5:c.-39+16873C>A (CYP19A1)	ENSP00000454004.1:n.-39+16873C>A
ENST00000558328.5:c.-39+16815C>A (CYP19A1)	ENSP00000453280.1:n.-39+16815C>A
ENST00000559980.5:c.-283+16196C>A (CYP19A1)	ENSP00000452872.1:n.-283+16196C>A
ENST00000561075.5:c.-39+16873C>A (CYP19A1)	ENSP00000454039.1:n.-39+16873C>A
NM_000103.3:c.-39+16873C>A (CYP19A1)	NP_000094.2:n.-39+16873C>A
NM_031226.2:c.-39+2194C>A (CYP19A1)	NP_112503.1:n.-39+2194C>A
XR_932224.1:n.3322G>T (PIRC66)
XR_932226.1:n.2615G>T (PIRC66)
XR_932229.1:n.6099G>T (PIRC66)
XR_932230.1:n.398G>T (PIRC66)
NM_001347248.1:c.-39+2194C>A (CYP19A1)	NP_001334177.1:n.-39+2194C>A
XR_002957708.1:n.378G>T
NM_000103.4:c.-39+16873C>A (CYP19A1) MANE Select	NP_000094.2:n.-39+16873C>A
NM_031226.3:c.-39+2194C>A (CYP19A1)	NP_112503.1:n.-39+2194C>A