Canonical Allele Identifier: CA1929297860
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94948767_94948776delinsCGTGAATGTA , CM000672.2:g.94948767_94948776delinsCGTGAATGTA GRCh38
NC_000010.10:g.96708524_96708533delinsCGTGAATGTA , CM000672.1:g.96708524_96708533delinsCGTGAATGTA GRCh37
NC_000010.9:g.96698514_96698523delinsCGTGAATGTA NCBI36
NG_008385.1:g.15110_15119delinsCGTGAATGTA
NG_008385.2:g.15610_15619delinsCGTGAATGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.643-341_643-332delinsCGTGAATGTA MANE Select ENSP00000260682.6:n.643-341_643-332delinsCGTGAATGTA
ENST00000643112.1:c.643-341_643-332delinsCGTGAATGTA ENSP00000496202.1:n.643-341_643-332delinsCGTGAATGTA
ENST00000260682.6:c.643-341_643-332delinsCGTGAATGTA ENSP00000260682.6:n.643-341_643-332delinsCGTGAATGTA
ENST00000473496.1:n.414-341_414-332delinsCGTGAATGTA
NM_000771.3:c.643-341_643-332delinsCGTGAATGTA NP_000762.2:n.643-341_643-332delinsCGTGAATGTA
NM_000771.4:c.643-341_643-332delinsCGTGAATGTA MANE Select NP_000762.2:n.643-341_643-332delinsCGTGAATGTA