Canonical Allele Identifier: CA15843105
Gene: CYP19A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51332881C>T , CM000677.2:g.51332881C>T GRCh38
NC_000015.9:g.51625078C>T , CM000677.1:g.51625078C>T GRCh37
NC_000015.8:g.49412370C>T NCBI36
NG_007982.1:g.10718G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396402.6:c.-39+5614G>A MANE Select ENSP00000379683.1:n.-39+5614G>A
ENST00000396402.5:c.-39+5614G>A ENSP00000379683.1:n.-39+5614G>A
ENST00000396404.8:c.-148+5614G>A ENSP00000379685.4:n.-148+5614G>A
ENST00000405011.6:c.-194+5614G>A ENSP00000384389.2:n.-194+5614G>A
ENST00000439712.6:c.-283+5614G>A ENSP00000390614.2:n.-283+5614G>A
ENST00000453807.6:c.-230+5614G>A ENSP00000391139.2:n.-230+5614G>A
ENST00000492852.1:n.87+5614G>A
ENST00000557858.5:c.-39+5614G>A ENSP00000452627.1:n.-39+5614G>A
ENST00000557934.5:c.-39+5614G>A ENSP00000454004.1:n.-39+5614G>A
ENST00000558328.5:c.-39+5556G>A ENSP00000453280.1:n.-39+5556G>A
ENST00000559980.5:c.-283+4937G>A ENSP00000452872.1:n.-283+4937G>A
ENST00000561075.5:c.-39+5614G>A ENSP00000454039.1:n.-39+5614G>A
NM_000103.3:c.-39+5614G>A NP_000094.2:n.-39+5614G>A
NM_031226.2:c.-148+5614G>A NP_112503.1:n.-148+5614G>A
NM_000103.4:c.-39+5614G>A MANE Select NP_000094.2:n.-39+5614G>A
NM_031226.3:c.-148+5614G>A NP_112503.1:n.-148+5614G>A
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