Canonical Allele Identifier: CA2789072436
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94948819_94948821dup , CM000672.2:g.94948819_94948821dup GRCh38
NC_000010.10:g.96708576_96708578dup , CM000672.1:g.96708576_96708578dup GRCh37
NC_000010.9:g.96698566_96698568dup NCBI36
NG_008385.1:g.15162_15164dup
NG_008385.2:g.15662_15664dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-289_643-287dup MANE Select ENSP00000260682.6:n.643-289_643-287dup
ENST00000643112.1:c.643-289_643-287dup ENSP00000496202.1:n.643-289_643-287dup
ENST00000260682.6:c.643-289_643-287dup ENSP00000260682.6:n.643-289_643-287dup
ENST00000473496.1:n.414-289_414-287dup
NM_000771.3:c.643-289_643-287dup NP_000762.2:n.643-289_643-287dup
NM_000771.4:c.643-289_643-287dup MANE Select NP_000762.2:n.643-289_643-287dup