Canonical Allele Identifier: CA2789073903
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988895del , CM000672.2:g.94988895del GRCh38
NC_000010.10:g.96748652del , CM000672.1:g.96748652del GRCh37
NC_000010.9:g.96738642del NCBI36
NG_008385.1:g.55238del
NG_008385.2:g.55738del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1340del MANE Select ENSP00000260682.6:p.Leu447TyrfsTer3
ENST00000643112.1:c.*349del ENSP00000496202.1:n.*349del
ENST00000260682.6:c.1340del ENSP00000260682.6:p.Leu447TyrfsTer3
NM_000771.3:c.1340del NP_000762.2:p.Leu447TyrfsTer3
NM_000771.4:c.1340del MANE Select NP_000762.2:p.Leu447TyrfsTer3