Canonical Allele Identifier: CA1929292408
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942220_94942221delinsGA , CM000672.2:g.94942220_94942221delinsGA GRCh38
NC_000010.10:g.96701977_96701978delinsGA , CM000672.1:g.96701977_96701978delinsGA GRCh37
NC_000010.9:g.96691967_96691968delinsGA NCBI36
NG_008385.1:g.8563_8564delinsGA
NG_008385.2:g.9063_9064delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.360_361delinsGA MANE Select ENSP00000260682.6:p.Trp120=
ENST00000643112.1:c.360_361delinsGA ENSP00000496202.1:p.Trp120=
ENST00000645207.1:n.513_514delinsGA
ENST00000260682.6:c.360_361delinsGA ENSP00000260682.6:p.Trp120=
ENST00000461906.1:n.385_386delinsGA
ENST00000473496.1:n.131_132delinsGA
NM_000771.3:c.360_361delinsGA NP_000762.2:p.Trp120=
NM_000771.4:c.360_361delinsGA MANE Select NP_000762.2:p.Trp120=