Canonical Allele Identifier: CA1929334771

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974502_94974503delinsAT , CM000672.2:g.94974502_94974503delinsAT	GRCh38
NC_000010.10:g.96734259_96734260delinsAT , CM000672.1:g.96734259_96734260delinsAT	GRCh37
NC_000010.9:g.96724249_96724250delinsAT	NCBI36
NG_008385.1:g.40845_40846delinsAT
NG_008385.2:g.41345_41346delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.961+2257_961+2258delinsAT MANE Select	ENSP00000260682.6:n.961+2257_961+2258delinsAT
ENST00000643112.1:c.820-6681_820-6680delinsAT	ENSP00000496202.1:n.820-6681_820-6680delinsAT
ENST00000260682.6:c.961+2257_961+2258delinsAT	ENSP00000260682.6:n.961+2257_961+2258delinsAT
NM_000771.3:c.961+2257_961+2258delinsAT	NP_000762.2:n.961+2257_961+2258delinsAT
NM_000771.4:c.961+2257_961+2258delinsAT MANE Select	NP_000762.2:n.961+2257_961+2258delinsAT