Canonical Allele Identifier: CA1929296231
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94947496_94947497delinsTA , CM000672.2:g.94947496_94947497delinsTA GRCh38
NC_000010.10:g.96707253_96707254delinsTA , CM000672.1:g.96707253_96707254delinsTA GRCh37
NC_000010.9:g.96697243_96697244delinsTA NCBI36
NG_008385.1:g.13839_13840delinsTA
NG_008385.2:g.14339_14340delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.482-283_482-282delinsTA MANE Select ENSP00000260682.6:n.482-283_482-282delins...
ENST00000643112.1:c.482-283_482-282delinsTA ENSP00000496202.1:n.482-283_482-282delins...
ENST00000645207.1:n.635-283_635-282delinsTA
ENST00000260682.6:c.482-283_482-282delinsTA ENSP00000260682.6:n.482-283_482-282delins...
ENST00000473496.1:n.253-283_253-282delinsTA
NM_000771.3:c.482-283_482-282delinsTA NP_000762.2:n.482-283_482-282delinsTA
NM_000771.4:c.482-283_482-282delinsTA MANE Select NP_000762.2:n.482-283_482-282delinsTA