Canonical Allele Identifier: CA2789072677
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942588del , CM000672.2:g.94942588del GRCh38
NC_000010.10:g.96702345del , CM000672.1:g.96702345del GRCh37
NC_000010.9:g.96692335del NCBI36
NG_008385.1:g.8931del
NG_008385.2:g.9431del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+247del MANE Select ENSP00000260682.6:n.481+247del
ENST00000643112.1:c.481+247del ENSP00000496202.1:n.481+247del
ENST00000645207.1:n.634+247del
ENST00000260682.6:c.481+247del ENSP00000260682.6:n.481+247del
ENST00000461906.1:n.753del
ENST00000473496.1:n.252+247del
NM_000771.3:c.481+247del NP_000762.2:n.481+247del
NM_000771.4:c.481+247del MANE Select NP_000762.2:n.481+247del