Canonical Allele Identifier: CA1929292109
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941752_94941753delinsGC , CM000672.2:g.94941752_94941753delinsGC GRCh38
NC_000010.10:g.96701509_96701510delinsGC , CM000672.1:g.96701509_96701510delinsGC GRCh37
NC_000010.9:g.96691499_96691500delinsGC NCBI36
NG_008385.1:g.8095_8096delinsGC
NG_008385.2:g.8595_8596delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-106_169-105delinsGC MANE Select ENSP00000260682.6:n.169-106_169-105delinsGC
ENST00000643112.1:c.169-106_169-105delinsGC ENSP00000496202.1:n.169-106_169-105delinsGC
ENST00000645207.1:n.216_217delinsGC
ENST00000260682.6:c.169-106_169-105delinsGC ENSP00000260682.6:n.169-106_169-105delinsGC
ENST00000461906.1:n.194-106_194-105delinsGC
NM_000771.3:c.169-106_169-105delinsGC NP_000762.2:n.169-106_169-105delinsGC
NM_000771.4:c.169-106_169-105delinsGC MANE Select NP_000762.2:n.169-106_169-105delinsGC