Canonical Allele Identifier: CA2789072438
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94948856_94948859del , CM000672.2:g.94948856_94948859del GRCh38
NC_000010.10:g.96708613_96708616del , CM000672.1:g.96708613_96708616del GRCh37
NC_000010.9:g.96698603_96698606del NCBI36
NG_008385.1:g.15199_15202del
NG_008385.2:g.15699_15702del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-252_643-249del MANE Select ENSP00000260682.6:n.643-252_643-249del
ENST00000643112.1:c.643-252_643-249del ENSP00000496202.1:n.643-252_643-249del
ENST00000260682.6:c.643-252_643-249del ENSP00000260682.6:n.643-252_643-249del
ENST00000473496.1:n.414-252_414-249del
NM_000771.3:c.643-252_643-249del NP_000762.2:n.643-252_643-249del
NM_000771.4:c.643-252_643-249del MANE Select NP_000762.2:n.643-252_643-249del