Canonical Allele Identifier: CA2789073904
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988942_94988944del , CM000672.2:g.94988942_94988944del GRCh38
NC_000010.10:g.96748699_96748701del , CM000672.1:g.96748699_96748701del GRCh37
NC_000010.9:g.96738689_96738691del NCBI36
NG_008385.1:g.55285_55287del
NG_008385.2:g.55785_55787del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1387_1389del MANE Select ENSP00000260682.6:p.Asp463del
ENST00000643112.1:c.*396_*398del ENSP00000496202.1:n.*396_*398del
ENST00000260682.6:c.1387_1389del ENSP00000260682.6:p.Asp463del
NM_000771.3:c.1387_1389del NP_000762.2:p.Asp463del
NM_000771.4:c.1387_1389del MANE Select NP_000762.2:p.Asp463del