Canonical Allele Identifier: CA2176808161
Gene: CYP19A1 HGNC NCBI
PIRC66 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51319392_51319394delinsCAA , CM000677.2:g.51319392_51319394delinsCAA GRCh38
NC_000015.9:g.51611589_51611591delinsCAA , CM000677.1:g.51611589_51611591delinsCAA GRCh37
NC_000015.8:g.49398881_49398883delinsCAA NCBI36
NG_007982.1:g.24205_24207delinsTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000396402.6:c.-39+19101_-39+19103delinsTTG (CYP19A1) MANE Select ENSP00000379683.1:n.-39+19101_-39+19103de...
ENST00000260433.6:c.-39+4422_-39+4424delinsTTG (CYP19A1) ENSP00000260433.2:n.-39+4422_-39+4424deli...
ENST00000396402.5:c.-39+19101_-39+19103delinsTTG (CYP19A1) ENSP00000379683.1:n.-39+19101_-39+19103de...
ENST00000396404.8:c.-39+4422_-39+4424delinsTTG (CYP19A1) ENSP00000379685.4:n.-39+4422_-39+4424deli...
ENST00000405011.6:c.-194+19101_-194+19103delinsTTG (CYP19A1) ENSP00000384389.2:n.-194+19101_-194+19103...
ENST00000439712.6:c.-283+19101_-283+19103delinsTTG (CYP19A1) ENSP00000390614.2:n.-283+19101_-283+19103...
ENST00000453807.6:c.-230+19101_-230+19103delinsTTG (CYP19A1) ENSP00000391139.2:n.-230+19101_-230+19103...
ENST00000492852.1:n.234-395_234-393delinsTTG (CYP19A1)
ENST00000557858.5:c.-39+19101_-39+19103delinsTTG (CYP19A1) ENSP00000452627.1:n.-39+19101_-39+19103de...
ENST00000557934.5:c.-39+19101_-39+19103delinsTTG (CYP19A1) ENSP00000454004.1:n.-39+19101_-39+19103de...
ENST00000558328.5:c.-39+19043_-39+19045delinsTTG (CYP19A1) ENSP00000453280.1:n.-39+19043_-39+19045de...
ENST00000559980.5:c.-283+18424_-283+18426delinsTTG (CYP19A1) ENSP00000452872.1:n.-283+18424_-283+18426...
ENST00000561075.5:c.-39+19101_-39+19103delinsTTG (CYP19A1) ENSP00000454039.1:n.-39+19101_-39+19103de...
NM_000103.3:c.-39+19101_-39+19103delinsTTG (CYP19A1) NP_000094.2:n.-39+19101_-39+19103delinsTT...
NM_031226.2:c.-39+4422_-39+4424delinsTTG (CYP19A1) NP_112503.1:n.-39+4422_-39+4424delinsTTG
XR_932224.1:n.3218-1557_3218-1555delinsCAA (PIRC66)
XR_932226.1:n.2511-1557_2511-1555delinsCAA (PIRC66)
XR_932229.1:n.5995-1557_5995-1555delinsCAA (PIRC66)
XR_932230.1:n.294-1557_294-1555delinsCAA (PIRC66)
NM_001347248.1:c.-39+4422_-39+4424delinsTTG (CYP19A1) NP_001334177.1:n.-39+4422_-39+4424delinsT...
NM_000103.4:c.-39+19101_-39+19103delinsTTG (CYP19A1) MANE Select NP_000094.2:n.-39+19101_-39+19103delinsTT...
NM_031226.3:c.-39+4422_-39+4424delinsTTG (CYP19A1) NP_112503.1:n.-39+4422_-39+4424delinsTTG