Canonical Allele Identifier: CA2518442646
Gene: CYP19A1 HGNC NCBI
PIRC66 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51302833_51302834insGAGCTTACTGTCTACTGGCAAAAAGTGCCGAGTACAGTTTCAACCCTTGAAATTGCCCTGGGTTGAAACTGTACT , CM000677.2:g.51302833_51302834insGAGCTTACTGTCTACTGGCAAAAAGTGCCGAGTACAGTTTCAACCCTTGAAATTGCCCTGGGTTGAAACTGTACT GRCh38
NC_000015.9:g.51595030_51595031insGAGCTTACTGTCTACTGGCAAAAAGTGCCGAGTACAGTTTCAACCCTTGAAATTGCCCTGGGTTGAAACTGTACT , CM000677.1:g.51595030_51595031insGAGCTTACTGTCTACTGGCAAAAAGTGCCGAGTACAGTTTCAACCCTTGAAATTGCCCTGGGTTGAAACTGTACT GRCh37
NC_000015.8:g.49382322_49382323insGAGCTTACTGTCTACTGGCAAAAAGTGCCGAGTACAGTTTCAACCCTTGAAATTGCCCTGGGTTGAAACTGTACT NCBI36
NG_007982.1:g.40800_40801insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000396402.6:c.-39+35696_-39+35697insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) MANE Select ENSP00000379683.1:n.-39+35696_-39+35697in...
ENST00000260433.6:c.-39+21017_-39+21018insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000260433.2:n.-39+21017_-39+21018in...
ENST00000396402.5:c.-39+35696_-39+35697insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000379683.1:n.-39+35696_-39+35697in...
ENST00000396404.8:c.-39+21017_-39+21018insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000379685.4:n.-39+21017_-39+21018in...
ENST00000405011.6:c.-193-24637_-193-24636insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000384389.2:n.-193-24637_-193-24636...
ENST00000439712.6:c.-283+35696_-283+35697insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000390614.2:n.-283+35696_-283+35697...
ENST00000453807.6:c.-230+35696_-230+35697insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000391139.2:n.-230+35696_-230+35697...
ENST00000557858.5:c.-39+35696_-39+35697insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000452627.1:n.-39+35696_-39+35697in...
ENST00000557934.5:c.-39+35696_-39+35697insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000454004.1:n.-39+35696_-39+35697in...
ENST00000558328.5:c.-39+35638_-39+35639insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000453280.1:n.-39+35638_-39+35639in...
ENST00000559646.1:c.-39+15634_-39+15635insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000453318.1:n.-39+15634_-39+15635in...
ENST00000559980.5:c.-283+35019_-283+35020insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000452872.1:n.-283+35019_-283+35020...
ENST00000561075.5:c.-39+35696_-39+35697insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) ENSP00000454039.1:n.-39+35696_-39+35697in...
NM_000103.3:c.-39+35696_-39+35697insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) NP_000094.2:n.-39+35696_-39+35697insAAACT...
NM_031226.2:c.-39+21017_-39+21018insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) NP_112503.1:n.-39+21017_-39+21018insAAACT...
XM_005254191.1:c.-39+15634_-39+15635insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) XP_005254248.1:n.-39+15634_-39+15635insAA...
XR_932223.1:n.5158_5159insGAGCTTACTGTCTACTGGCAAAAAGTGCCGAGTACAGTTTCAACCCTTGAAATTGCCCTGGGTTGAAACTGTACT (PIRC66)
XR_932229.1:n.5158_5159insGAGCTTACTGTCTACTGGCAAAAAGTGCCGAGTACAGTTTCAACCCTTGAAATTGCCCTGGGTTGAAACTGTACT (PIRC66)
NM_001347248.1:c.-39+21017_-39+21018insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) NP_001334177.1:n.-39+21017_-39+21018insAA...
NM_001347249.1:c.-39+15634_-39+15635insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) NP_001334178.1:n.-39+15634_-39+15635insAA...
NM_000103.4:c.-39+35696_-39+35697insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) MANE Select NP_000094.2:n.-39+35696_-39+35697insAAACT...
NM_001347249.2:c.-39+15634_-39+15635insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) NP_001334178.1:n.-39+15634_-39+15635insAA...
NM_031226.3:c.-39+21017_-39+21018insAAACTGTACTCGGCACTTTTTGCCAGTAGACAGTAAGCTCAGTACAGTTTCAACCCAGGGCAATTTCAAGGGTTG (CYP19A1) NP_112503.1:n.-39+21017_-39+21018insAAACT...