Canonical Allele Identifier: CA2838797385
Gene: CYP2C9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981232dup , CM000672.2:g.94981232dup GRCh38
NC_000010.10:g.96740989dup , CM000672.1:g.96740989dup GRCh37
NC_000010.9:g.96730979dup NCBI36
NG_008385.1:g.47575dup
NG_008385.2:g.48075dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1011dup MANE Select ENSP00000260682.6:p.Cys338LeufsTer23
ENST00000643112.1:c.*20dup ENSP00000496202.1:n.*20dup
ENST00000260682.6:c.1011dup ENSP00000260682.6:p.Cys338LeufsTer23
NM_000771.3:c.1011dup NP_000762.2:p.Cys338LeufsTer23
NM_000771.4:c.1011dup MANE Select NP_000762.2:p.Cys338LeufsTer23
Search 100 bp 5'
Search 100 bp 3'